The Upjohn Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
The Upjohn Co. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
The Upjohn Co. has 6 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 6 cleared submissions from 1976 to 1990. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by The Upjohn Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - The Upjohn Co.
6 devices
Cleared
May 15, 1990
TROBICIN SUSCEPTIBILITY POWDER
Microbiology
39d
Cleared
Feb 09, 1990
ZEFAZONE SUSCEPTIBILITY POWDER
Microbiology
10d
Cleared
May 29, 1981
CK-TOTAL/CK-B (NAC) BIOLUMIN. ASSAY KIT
Chemistry
60d
Cleared
Mar 02, 1979
RIA KIT, PROGESTERONE
Chemistry
91d
Cleared
Jun 13, 1978
TESTOSTERONE RADIOIMMUNOASSAY KIT 125I
Immunology
29d
Cleared
Nov 09, 1976
CAT-A-KIT
Chemistry
12d