Palmetto Chemical & Supply Co., Inc.: FDA clearances and approvals

Palmetto Chemical & Supply Co., Inc. has 6 FDA 510(k) clearances (first 1986, latest 1986), across 2 product codes in 1 review panel. Median 510(k) review time: 36 days.

510(k) clearances per year

YearClearancesMedian review days
20120—
20130—
20140—
20150—
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20170—
20180—
20190—
20200—
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20220—
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20250—
20260—

Top product codes

Product codeDeviceSubmissions510(k) clearances
FLGCleaner, Ultrasonic, Medical Instrument44

Plus 1 more product codes.

Review panels

Most recent Palmetto Chemical & Supply Co., Inc. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K861592WEC-WASH, CATALOG NO. 850-115FLG1986-06-1749
K861590WEC-KLEEN, CATALOG N. 850-102FLG1986-06-1749
K861588WECK INSTRUMENT CLEANER, CAT. NO. 850-103FLG1986-06-1749
K861591WECK-LUBE, CATALOG NO. 850-150—1986-05-2324
K861589WECK-KREEM, CATALOG NO. 850-155—1986-05-2324
K861587WECK CONCENTRATED LIQUID CLEANERFLG1986-05-1920

Recalls

openFDA lists no recalls under a recalling firm named Palmetto Chemical & Supply Co., Inc..

Recalling firms are matched to this company by name only (same normalization as the applicant), so related entities that recall under another name are not counted.

Frequently asked questions

How many FDA 510(k) clearances does Palmetto Chemical & Supply Co., Inc. have?

Palmetto Chemical & Supply Co., Inc. has 6 FDA 510(k) clearances (first 1986, latest 1986), across 2 product codes in 1 review panel.

How long does FDA take to clear Palmetto Chemical & Supply Co., Inc.'s 510(k)s?

The median time from FDA receipt to decision across Palmetto Chemical & Supply Co., Inc.'s cleared 510(k)s is 36 days.

What devices does Palmetto Chemical & Supply Co., Inc. make?

Its most frequent FDA product codes are FLG (Cleaner, Ultrasonic, Medical Instrument, 4).

Has Palmetto Chemical & Supply Co., Inc. had device recalls?

openFDA lists no recalls under a recalling firm name matching Palmetto Chemical & Supply Co., Inc. Related entities may recall under other names.

Next steps

Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Companies are grouped by FDA applicant name with punctuation and legal suffixes removed. Review days run from FDA receipt to decision. Not regulatory advice.

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