Ppg Industries, Inc.
Pleasantville, NY, US
Ppg Industries, Inc. appears in FDA device records in Pleasantville, NY. FDA records list 20 510(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
- 20
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 20 510(k) clearances for Ppg Industries, Inc. between 1987 and 1992. The busiest year on record is 1990, with 6. The most recent is 1992, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1987 | 1 |
| 1988 | 5 |
| 1989 | 4 |
| 1990 | 6 |
| 1991 | 3 |
| 1992 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K922631 | STATPAL II BLOOD GAS ANALYSIS SYSTEM | CHL | Substantially Equivalent | |
| K913358 | MIDAS SYSTEM(TM) 5100 PHYSIOLOG MONIT/RECORD SYST | DXG | Substantially Equivalent | |
| K914560 | STAT PAL SENSYR SYRINGE ASSEMBLY FOR USE W/STATPAL | CHL | Substantially Equivalent | |
| K912627 | MIDAS SYSTEM 2500, PHYSIOLOGICAL MONITORING SYSTEM | MHX | Substantially Equivalent | |
| K903965 | STATPAL BLOOD GAS MONITORING SYSTEM | CHL | Substantially Equivalent | |
| K901514 | XR MODEL H PHYSIOLOGICAL MONITOR & RECORDING SYS. | DSK | Substantially Equivalent | |
| K900246 | CARDIOTEST EK 53 R, CARDIOGNOST EK 56/ EK 512 | DSI | Substantially Equivalent | |
| K901132 | SARA SATCAP | CCK | Substantially Equivalent | |
| K896442 | PPG BIOMEDICAL VENTILATOR MODEL IRISA | CBK | Substantially Equivalent | |
| K900700 | SMU 611 UNIVERSALMONITOR | DPS | Substantially Equivalent | |
| K890875 | CARDIOTEST EK53/EK53R, CARDIOGNOST EK56/EK512 | DPS | Substantially Equivalent | |
| K894286 | PPG BIOMEDICAL FLEXIBLE MICRO TRANSDUCER CATHETER | DXO | Substantially Equivalent | |
| K890725 | PHOTOCHROMIC LENS | HQY | Substantially Equivalent | |
| K884158 | THE SYSTEM, SARA DIGICAP PLUS OHMEDA MINX OXIMETER | CCK | Substantially Equivalent | |
| K880505 | ECG/RESPIRATION/ARRHYTHMIA MODULE FOR RM-301 | DSI | Substantially Equivalent | |
| K883436 | PPG BIOMEDICAL FLEXIBLE MICRO TRANSDUCER CATHETER | DXO | Substantially Equivalent | |
| K880879 | WORKSTATION PLUS W/LOCAL AREA NETWORK(LAN) OPTION | DQK | Substantially Equivalent | |
| K880498 | RM-301 PATIENT MONITOR | DRT | Substantially Equivalent | |
| K875265 | NON-INVASIVE BLOOD PRESSURE MODULE | DXN | Substantially Equivalent | |
| K871433 | PPG BIOMEDICAL VENTILATOR MODEL AV 400 | CBK | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- CCKAnalyzer, Gas, Carbon-Dioxide, Gaseous-Phase
- DSKComputer, Blood-Pressure
- DXGComputer, Diagnostic, Pre-Programmed, Single-Function
- DQKComputer, Diagnostic, Programmable
- DSIDetector And Alarm, Arrhythmia
- DPSElectrocardiograph
- CHLElectrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph
- DRTMonitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
- MHXMonitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
- HQYSunglasses (Non-Prescription Including Photosensitive)
- DXNSystem, Measurement, Blood-Pressure, Non-Invasive
- DXOTransducer, Pressure, Catheter Tip
- CBKVentilator, Continuous, Facility Use
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