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.
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