Phoenix Glove Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Phoenix Glove Co. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Phoenix Glove Co. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1978 to 1983. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Phoenix Glove Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Phoenix Glove Co.
6 devices
Cleared
Mar 17, 1983
STERILE SURGICAL DRAPES
General Hospital
15d
Cleared
Jun 23, 1982
PATIENT PREP KITS/TRAYS-STERILE
General Hospital
70d
Cleared
Jun 21, 1982
STERILE SURGICAL DRAPES
Gastroenterology & Urology
14d
Cleared
May 21, 1982
STERILE PATIENT EXAM. GLOVES
General Hospital
37d
Cleared
Sep 09, 1980
ELECTROCARDIOGRAPH ELECTRODE
Cardiovascular
36d
Cleared
Dec 07, 1978
GLOVES, VINYL EXAMINATION
General Hospital
41d