J. H. Emerson Co.
Cambridge, MA, US
J. H. Emerson Co. appears in FDA device records in Cambridge, MA. FDA records list 25 510(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
- 25
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 25 510(k) clearances for J. H. Emerson Co. between 1981 and 2000. The busiest year on record is 1981, with 4. The most recent is 2000, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1981 | 4 |
| 1982 | 1 |
| 1983 | 2 |
| 1984 | 3 |
| 1985 | 2 |
| 1986 | 4 |
| 1987 | 3 |
| 1988 | 1 |
| 1990 | 2 |
| 1992 | 1 |
| 1993 | 1 |
| 2000 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K002598 | EMERSON COUGH ASSIST MODEL CA-3000 W/AUTOMATIC TIMING AND MODEL CM-3000 W/MANUAL TIMING | NHJ | Substantially Equivalent | |
| K920910 | OXYGEN POWERED RESUSCITATOR FOR CPR | BTL | Substantially Equivalent | |
| K924174 | EMERSON IN-EXSUFFLATOR, MODELS 2-CM & 2-CA | NHJ | Substantially Equivalent | |
| K902764 | EMERSON 33-AN NEGATIVE PRESSURE RESPIRATOR ALARM | BYT | Substantially Equivalent | |
| K896721 | MODEL 7-AT TREATMENT CHAMBER | LGM | Substantially Equivalent | |
| K881808 | EMERSON CHEST RESPIRATOR, MODEL 33-CRE | BYT | Substantially Equivalent | |
| K873489 | EMERSON DISPOS THORACIC DRAINAGE SET - 551-8000 | GCX | Substantially Equivalent | |
| K872937 | 97-TD EMERSON TIMER/DIMMER CONTROL | IQA | Substantially Equivalent | |
| K872936 | 97-D EMERSON DIMMER CONTROL | IQA | Substantially Equivalent | |
| K864379 | EMERSON 3MV VOLUME VENTILATOR | CBK | Substantially Equivalent | |
| K864394 | EMERSON 3MV VOLUME VENTILATOR | Substantially Equivalent | ||
| K862712 | EMERSON MODEL 3HV COMPACT VENTILATOR | CBK | Substantially Equivalent | |
| K853132 | EMERSON TRO/CATH TROCAR CATHETERS | DRC | Substantially Equivalent | |
| K854799 | EMERSON MODEL 3MV-OAA ALARM MODULE | CCL | Substantially Equivalent | |
| K853131 | THORO/CATH STRAIGHT THORACIC RIGHT ANGLE | GBS | Substantially Equivalent | |
| K842604 | EMERSON MOTION BED 6-MS & 6-ME | IKZ | Substantially Equivalent | |
| K842488 | SAMSON 1000 ANESTHESIA CIRCUIT | CAI | Substantially Equivalent | |
| K842487 | SAMSON'S NEWBORN LUNG INFLATOR 340-1000 | BTM | Substantially Equivalent | |
| K832271 | EMERSON MODEL 3MV-AP AND 3V-AP PRESS- | CAP | Substantially Equivalent | |
| K832176 | NEGATIVE PRESSURE CHEST RESPIRATOR PUMP | BYT | Substantially Equivalent | |
| K820077 | EMERSON THORACIC SUCTION REG. #55-JP | KDP | Substantially Equivalent | |
| K813319 | ASPIRATOR VENTURI SYSTEM MODEL 55-JV | GCX | Substantially Equivalent | |
| K812745 | WARMING LISTHTS #96H & 96HT | FMT | Substantially Equivalent | |
| K812746 | THORACIC DRAINAGE SET #55-DB2-G | KDQ | Substantially Equivalent | |
| K811779 | ROSS-EMERSON PUMP, MODEL 55-R | KQT | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- CCLAnalyzer, Gas, Oxygen, Gaseous-Phase
- GCXApparatus, Suction, Operating-Room, Wall Vacuum Powered
- IKZBed, Patient Rotation, Powered
- KDQBottle, Collection, Vacuum
- GBSCatheter, Ventricular, General & Plastic Surgery
- LGMChamber, Patient Isolation
- CAICircuit, Breathing (W Connector, Adaptor, Y Piece)
- NHJDevice, Positive Pressure Breathing, Intermittent
- KQTEvacuator, Gastro-Urology
- CAPMonitor, Airway Pressure (Includes Gauge And/Or Alarm)
- KDPRegulator, Vacuum
- IQASystem, Environmental Control, Powered
- DRCTrocar
- CBKVentilator, Continuous, Facility Use
- BTMVentilator, Emergency, Manual (Resuscitator)
- BTLVentilator, Emergency, Powered (Resuscitator)
- BYTVentilator, External Body, Negative Pressure, Adult (Cuirass)
- FMTWarmer, Infant Radiant
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain
