Medical Device Manufacturer · US , New York , NY

E. R. Squibb & Sons, Inc. - FDA 510(k) Cleared Devices

32 submissions · 32 cleared · Since 1977

Total

Cleared

Denied

E. R. Squibb & Sons, Inc. has 32 FDA 510(k) cleared medical devices. Based in New York, US.

Historical record: 32 cleared submissions from 1977 to 1982. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by E. R. Squibb & Sons, Inc. Filter by specialty or product code using the sidebar.

E. R. Squibb & Sons, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - E. R. Squibb & Sons, Inc.

32 devices

1-12 of 32

ANGIOTENSIS I-SQUIBB RADIOIMMUNOASSAY

K820616 · CIB

Toxicology · 18d

Cleared Mar 04, 1982

T3 UPTAKE-SQUIBB DIAGNOSTIC KIT

K820340 · KHQ

Toxicology · 24d

Cleared Mar 04, 1982

CORTISOL-SQUIBB RADIOIMMUNOASSAY KIT

K820341 · CGR

Toxicology · 24d

Cleared Jun 16, 1981

SUR-FIT LOOP OSTOMY O.R. SET

K811240 · EXB

Gastroenterology & Urology · 43d

Cleared Jun 09, 1981

SUR-FIT DISPOSABLE CONVEX INSERT

K811239 · EXB

Gastroenterology & Urology · 36d

Cleared Jun 02, 1981

SUR-FIT IRRIGATION SLEEVE

K811160 · EXD

Gastroenterology & Urology · 35d

Cleared May 21, 1981

SUR-FIT DISPOSABLE FANGE CAP

K811163 · EXB

Gastroenterology & Urology · 23d

Cleared Apr 21, 1981

DIAGOXIN SQUIBB RADIOIMMUNOASSAY KIT

STOMAHESIVE PASTE PROTECTIVE SKIN BARR

K803100 · EZR

Gastroenterology & Urology · 30d

E. R. Squibb & Sons, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - E. R. Squibb & Sons, Inc.

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