Zimmer Patient Care Division is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Zimmer Patient Care Division - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Zimmer Patient Care Division has 3 FDA 510(k) cleared medical devices. Based in Dover, US.
Historical record: 3 cleared submissions from 1993 to 1996.
Browse the FDA 510(k) cleared devices submitted by Zimmer Patient Care Division Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Zimmer Patient Care Division
3 devices
Cleared
Nov 06, 1996
ECONOMY SAFETY VEST RESTRAINT, SHOULDER TIE SAFETY VEST/SAFETY VEST...
General Hospital
68d
Cleared
Jan 31, 1994
GENERAL SURGERY PROBE/GENERAL SURGERY PROBE W/DISTAL PERFORATIONS
General & Plastic Surgery
62d
Cleared
Jan 28, 1993
HEMOVAC AUTOTRANSFUSION SYSTEM
Anesthesiology
372d