Medical Device Manufacturer · US , New York , NY

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

32 submissions · 32 cleared · Since 1977

32

Total

32

Cleared

0

Denied

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

11 devices

1-11 of 11

Cleared Mar 26, 1982

ANGIOTENSIS I-SQUIBB RADIOIMMUNOASSAY

Toxicology · 18d

Cleared Mar 04, 1982

T3 UPTAKE-SQUIBB DIAGNOSTIC KIT

Toxicology · 24d

Cleared Mar 04, 1982

CORTISOL-SQUIBB RADIOIMMUNOASSAY KIT

Toxicology · 24d

Cleared Apr 21, 1981

DIAGOXIN SQUIBB RADIOIMMUNOASSAY KIT

Toxicology · 13d

Cleared Feb 10, 1981

Toxicology · 15d

Cleared May 08, 1980

DIGOXIN CLASP RIA KIT

Toxicology · 13d

Cleared Apr 04, 1979

CORTISOL RIA KIT

Toxicology · 58d

Cleared Oct 24, 1978

ASSAY SYSTEM, GAMMAFLO, AUTOMATED

Toxicology · 26d

Cleared Oct 24, 1978

Toxicology · 26d

Cleared Jul 14, 1977

T3 CLASP RIA KIT

Toxicology · 17d

Cleared Jan 18, 1977

DIGOXIN CLASP TM RIA KIT

Toxicology · 5d