Pfizer Pharmaceuticals is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pfizer Pharmaceuticals - FDA 510(k) Cleared Devices
6
Total
5
Cleared
0
Denied
Pfizer Pharmaceuticals has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1977 to 1989.
Browse the FDA 510(k) cleared devices submitted by Pfizer Pharmaceuticals Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pfizer Pharmaceuticals
6 devices
Cleared
Mar 22, 1989
WATER JEL STERILE GEL-SOAKED BURN DRESSING
General & Plastic Surgery
84d
Cleared
Mar 31, 1981
CEFOTAXIME 30MCG ANTIMICROBIAL SUSCEP.
Microbiology
41d
Cleared
Oct 23, 1980
E-VAC BLOOD CULTURE SYSTEM
Microbiology
20d
Cleared
Sep 15, 1977
CREATINE KINASE ISOENZYME SUBSTRATE SET
Chemistry
24d
Cleared
May 25, 1977
MICROBIO. PROD. FLUORESCENT ANTIBODY
Immunology
23d
Cleared
Apr 15, 1977
NEEDLES, STERILE, AIRWAY
General Hospital
39d