Surgipro, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Surgipro, Inc. - FDA 510(k) Cleared Devices
5
Total
0
Cleared
0
Denied
Surgipro, Inc. has 0 FDA 510(k) cleared medical devices. Based in Palm Harbor, US.
Historical record: 0 cleared submissions from 1993 to 1994. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Surgipro, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Surgipro, Inc.
5 devices
Cleared
Mar 01, 1994
STERILE CENTRAL LINE DRESSING TRAY
General Hospital
196d
Cleared
Feb 17, 1994
STERILE DRESSING CHANGE TRAY
General Hospital
184d
Cleared
Feb 04, 1994
STERILE LACERATION & DEBRIDEMENT TRAYS
General & Plastic Surgery
171d
Cleared
Jan 26, 1994
STERILE TRACHEOSTOMY TRAY
General & Plastic Surgery
162d
Cleared
Jun 17, 1993
VARIOUS STERILE CUSTOM DRESSING TRAYS & KITS
General Hospital
751d