Ppg Industries, Inc.: FDA filings under this applicant name
FDA lists 20 510(k) clearances under the applicant name “Ppg Industries, Inc.” (first 1987, latest 1992), across 13 product codes in 4 review panels. Median 510(k) review time under this name: 102 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| CHL | Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph | 3 | 3 |
| CBK | Ventilator, Continuous, Facility Use | 2 | 2 |
| CCK | Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase | 2 | 2 |
| DPS | Electrocardiograph | 2 | 2 |
| DSI | Detector And Alarm, Arrhythmia | 2 | 2 |
| DXO | Transducer, Pressure, Catheter Tip | 2 | 2 |
| DQK | Computer, Diagnostic, Programmable | 1 | 1 |
| DRT | Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm) | 1 | 1 |
| DSK | Computer, Blood-Pressure | 1 | 1 |
| DXG | Computer, Diagnostic, Pre-Programmed, Single-Function | 1 | 1 |
Plus 3 more product codes.
Review panels
- Cardiovascular (12)
- Anesthesiology (4)
- Clinical Chemistry (3)
- Ophthalmic (1)
Most recent Ppg Industries, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K922631 | STATPAL II BLOOD GAS ANALYSIS SYSTEM | CHL | 1992-11-10 | 160 |
| K913358 | MIDAS SYSTEM(TM) 5100 PHYSIOLOG MONIT/RECORD SYST | DXG | 1991-12-20 | 144 |
| K914560 | STAT PAL SENSYR SYRINGE ASSEMBLY FOR USE W/STATPAL | CHL | 1991-11-29 | 45 |
| K912627 | MIDAS SYSTEM 2500, PHYSIOLOGICAL MONITORING SYSTEM | MHX | 1991-09-10 | 88 |
| K903965 | STATPAL BLOOD GAS MONITORING SYSTEM | CHL | 1990-12-26 | 120 |
| K901514 | XR MODEL H PHYSIOLOGICAL MONITOR & RECORDING SYS. | DSK | 1990-11-16 | 231 |
| K900246 | CARDIOTEST EK 53 R, CARDIOGNOST EK 56/ EK 512 | DSI | 1990-07-03 | 167 |
| K901132 | SARA SATCAP | CCK | 1990-05-22 | 71 |
| K896442 | PPG BIOMEDICAL VENTILATOR MODEL IRISA | CBK | 1990-04-16 | 158 |
| K900700 | SMU 611 UNIVERSALMONITOR | DPS | 1990-04-03 | 50 |
10 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Ppg Industries, Inc..
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
SEC filings
PPG INDUSTRIES INC (PPG): EDGAR filings, CIK 79879. An SEC registrant with the same name, matched by name only.
Frequently asked questions
How many FDA 510(k) clearances are listed under Ppg Industries, Inc.?
FDA lists 20 510(k) clearances under the applicant name “Ppg Industries, Inc.” (first 1987, latest 1992), across 13 product codes in 4 review panels. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Ppg Industries, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Ppg Industries, Inc. is 102 days.
Which FDA product codes appear under Ppg Industries, Inc.?
The most frequent FDA product codes under this applicant name are CHL (Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph, 3); CBK (Ventilator, Continuous, Facility Use, 2); CCK (Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase, 2).
Next steps
- See all 20 Ppg Industries, Inc. clearances with predicates and recalls
- Run predicate analysis for product code CHL, Ppg Industries, Inc.'s most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.