Medical Device Manufacturer · US , Mchenry , IL

G.D. Searle and Co. - FDA 510(k) Cleared Devices

56 submissions · 56 cleared · Since 1976

Total

Cleared

Denied

G.D. Searle and Co. has 56 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 56 cleared submissions from 1976 to 1982.

Browse the FDA 510(k) cleared devices submitted by G.D. Searle and Co. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - G.D. Searle and Co.

56 devices

1-12 of 56

Cleared May 25, 1982

IN-LINE OXYGEN MONITORING SYSTEM

INTRAVASCULAR CATHETER

K803238 · FOZ

General Hospital · 121d

Cleared Mar 31, 1981

SILICONE ELASTOMER COATED LATEX FOLEY

K810630 · KOD

Gastroenterology & Urology · 22d

Cleared Feb 26, 1981

ADMINISTRATION SET

K810131 · FPD

Gastroenterology & Urology · 38d

Cleared Feb 12, 1981

SEARLE VASCULAR LOOPS

K802485 · KDC

General & Plastic Surgery · 125d

SWR DISPOSABLE PREP RAZOR

K810112 · KDC

General & Plastic Surgery · 19d

Cleared Oct 10, 1980

WHITE KNIGHT BOVIE CORD/SUCTION TUBE

K802213 · KKX

General Hospital · 28d

Cleared Oct 10, 1980

WHITE KNIGHT DRAPE SEAL

K802280 · KKX

General Hospital · 22d

Cleared Aug 20, 1980

LATEX FOLEY CATHETER (HYDROMER COATED)

K801415 · KOD

Gastroenterology & Urology · 65d

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G.D. Searle and Co. - FDA 510(k) Cleared Devices

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