Honeywell, Inc.
Mchenry, IL, US
Honeywell, Inc. appears in FDA device records in Mchenry, IL. FDA records list 69 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 69
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
Showing 50 of 69FDA records hold 69 510(k) clearances for Honeywell, Inc. between 1976 and 1990. The busiest year on record is 1981, with 26. The most recent is 1990, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1976 | 2 |
| 1977 | 10 |
| 1978 | 4 |
| 1979 | 3 |
| 1980 | 2 |
| 1981 | 26 |
| 1982 | 3 |
| 1983 | 8 |
| 1984 | 3 |
| 1985 | 4 |
| 1986 | 2 |
| 1987 | 1 |
| 1990 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K902230 | COLORADO COLOR IMAGING RECORDER | DSF | Substantially Equivalent | |
| K863100 | CEN STA MON AC/DC ALARM CENTRAL ACCES ALARM RECOR | DPS | Substantially Equivalent | |
| K853501 | HONEYWELL ELECTRONIC VENTILATOR EV-A | CBK | Substantially Equivalent | |
| K855125 | PHYSIOLOGICAL TELEMETRY PATIENT MONITORING SYSTEM | DRT | Substantially Equivalent | |
| K851888 | APM DISPOS. BLOOD PRESSURE TRANSDUCER | DRS | Substantially Equivalent | |
| K851496 | ECG MONITOR MODEL RM102 | DXJ | Substantially Equivalent | |
| K850794 | PATIENT MONITOR MODEL RM-300 | DTR | Substantially Equivalent | |
| K851092 | PORTABLE DEFIBRILLATOR/MONITOR ED 425 | LDD | Substantially Equivalent | |
| K834530 | EXTENSION BOX EB200 | DRT | Substantially Equivalent | |
| K834282 | ULTRA IMAGER 2000 | IYO | Substantially Equivalent | |
| K840167 | PORTABLE DEFIBRILLATOR | LDD | Substantially Equivalent | |
| K831164 | PATIENT MONITOR CM 135 | DRT | Substantially Equivalent | |
| K831696 | PORTABLE DEFIBRILLATOR MONITOR 74DRK | LDD | Substantially Equivalent | |
| K831818 | CENTRAL STATION MONITOR CSM-100 | DRT | Substantially Equivalent | |
| K831817 | PATIENT MONITOR #RM-100 | DRT | Substantially Equivalent | |
| K832212 | PATIENT SELECTOR FUNCTION BLOCK | DPS | Substantially Equivalent | |
| K830914 | EXTERNAL VALVE FUNCTION BLOCK | DRQ | Substantially Equivalent | |
| K830566 | CONVERTER UNIT FOR ECG TRACE DISPLAY | DPS | Substantially Equivalent | |
| K830779 | PRESSURE FUNCTION BLOCK FOR BLOOD PRESS | DRT | Substantially Equivalent | |
| K822926 | MODEL LS-85 & MEDEL 1828 LINESCAN VISCO | Substantially Equivalent | ||
| K827408 | ULTRA IMAGER | Substantially Equivalent | ||
| K822590 | PRESSURE ISOLATION AMPLIFIER #9813 517 | DRJ | Substantially Equivalent | |
| K813064 | TELEMETRY TRANSMITTER & RECEIVER | DRG | Substantially Equivalent | |
| K813125 | MICRO TRANSDUCER CATHETERS | DRE | Substantially Equivalent | |
| K812667 | MEDDARS/ULTRA IMAGER RESPIRATION MODULE | BZQ | Substantially Equivalent | |
| K812103 | ESOPHAGEAL MOTILITY APPARATUS | FFX | Substantially Equivalent | |
| K811581 | ARRHYTHMIA FUNCTION BLOCK | DSI | Substantially Equivalent | |
| K811626 | MEDDARS/ULTRA IMAGER PULSE/PHON MODULE | DQC | Substantially Equivalent | |
| K810696 | PHYSIOLOGIC RECORDER | DPS | Substantially Equivalent | |
| K810175 | NEO NATAL RESPIRATION FUNCTION BLOCK | BZQ | Substantially Equivalent | |
| K810174 | RESPIRATION FUNCTION BLOCKS | BZQ | Substantially Equivalent | |
| K810163 | AM 420 MICROPROCESSOR | DXG | Substantially Equivalent | |
| K810179 | DUAL TRACE PATIENT MONITOR 116,118,120 | DSK | Substantially Equivalent | |
| K810178 | PATIENT MONITOR CM111, 112 | DSK | Substantially Equivalent | |
| K810177 | PATIENT MONITOR MODEL CM130, 140 | DXG | Substantially Equivalent | |
| K810176 | ECG FUNCTION BLOCK | DPS | Substantially Equivalent | |
| K810172 | PRESSURE FUNCTION BLOCKS | DSK | Substantially Equivalent | |
| K810171 | PERIPHERAL PULSE FUNCTION BLOCKS | DSK | Substantially Equivalent | |
| K810170 | TREND GRAPH FUNCTION BLOCK | DXG | Substantially Equivalent | |
| K810169 | CENTRAL STATION CONTROLLER AC100/CE100 | DSF | Substantially Equivalent | |
| K810168 | SLAVE MONITORS DC109 & VS109 | DXJ | Substantially Equivalent | |
| K810167 | SINGLE CHANNELL RECORDER AR110 | DSF | Substantially Equivalent | |
| K810166 | 1,2,3 CHANNELL RECORDERS (AR150,AR250,-) | DSF | Substantially Equivalent | |
| K810165 | DUAL TRACE VIDEO MONITOR VM 410 | DXJ | Substantially Equivalent | |
| K810164 | VC 430 VIDEO CONVERTER | DXJ | Substantially Equivalent | |
| K810263 | MICROPROCESSOR CONTROLLED ELECTROCARDIO | DPS | Substantially Equivalent | |
| K810237 | PORTABLE, BATTERY OPERATED DEFIBRILLATOR | LDD | Substantially Equivalent | |
| K810173 | TEMPERATURE FUNCTION BLOCK | FLL | Substantially Equivalent | |
| K800553 | ULTRA IMAGER | DXK | Substantially Equivalent | |
| K792677 | DATABASE MANAGEMENT & REPORTING SYSTEM | DQK | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- DRQAmplifier And Signal Conditioner, Transducer Signal
- GWLAmplifier, Physiological Signal
- DSKComputer, Blood-Pressure
- DXGComputer, Diagnostic, Pre-Programmed, Single-Function
- DQKComputer, Diagnostic, Programmable
- FLLContinuous Measurement Thermometer
- LDDDc-Defibrillator, Low-Energy, (Including Paddles)
- DSIDetector And Alarm, Arrhythmia
- JOYDevice, Automated Cell-Locating
- DREDilator, Vessel, For Percutaneous Catheterization
- DXJDisplay, Cathode-Ray Tube, Medical
- DXKEchocardiograph
- DPSElectrocardiograph
- DTRHeat-Exchanger, Cardiopulmonary Bypass
- BZQMonitor, Breathing Frequency
- DRTMonitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
- DQCPhonocardiograph
- CCMPlethysmograph, Pressure
- DSFRecorder, Paper Chart
- KPASlide Stainer, Automated
- KEYStainer, Tissue, Automated
- FFXSystem, Gastrointestinal Motility (Electrical)
- IYOSystem, Imaging, Pulsed Echo, Ultrasonic
- DRJSystem, Signal Isolation
- IYMSystem, Telethermographic, Infrared
- DRSTransducer, Blood-Pressure, Extravascular
- DRGTransmitters And Receivers, Physiological Signal, Radiofrequency
- CBKVentilator, Continuous, Facility Use
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain
