Ppg/Applied Resources, Inc.: FDA filings under this applicant name

FDA lists 5 510(k) clearances under the applicant name “Ppg/Applied Resources, Inc.” (first 1988, latest 1988), across 1 product code in 1 review panel. Median 510(k) review time under this name: 124 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

YearClearancesMedian review days
20120—
20130—
20140—
20150—
20160—
20170—
20180—
20190—
20200—
20210—
20220—
20230—
20240—
20250—
20260—

Top product codes

Product codeDeviceSubmissions510(k) clearances
CCKAnalyzer, Gas, Carbon-Dioxide, Gaseous-Phase55

Review panels

Most recent Ppg/Applied Resources, Inc. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K881002O.R. SARACAPCCK1988-08-15159
K882172SARACAP AGCCK1988-06-2431
K881093ICU SARACAPCCK1988-06-24101
K874724SARA AGIE MONITORCCK1988-03-29132
K874754SARA DIGICAPCCK1988-03-21124

Recalls

openFDA lists no recalls under a recalling firm named Ppg/Applied Resources, 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.

Frequently asked questions

How many FDA 510(k) clearances are listed under Ppg/Applied Resources, Inc.?

FDA lists 5 510(k) clearances under the applicant name “Ppg/Applied Resources, Inc.” (first 1988, latest 1988), across 1 product code in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.

How long has FDA taken to clear 510(k)s filed by Ppg/Applied Resources, Inc.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Ppg/Applied Resources, Inc. is 124 days.

Which FDA product codes appear under Ppg/Applied Resources, Inc.?

The most frequent FDA product codes under this applicant name are CCK (Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase, 5).

Next steps

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.

All FDA device companies · FDA product code lookup