North American Sterilization & Packaging Co. - FDA 510(k) Cleared Dev...
16
Total
16
Cleared
0
Denied
North American Sterilization & Packaging Co. has 16 FDA 510(k) cleared medical devices. Based in Sparta, US.
Historical record: 16 cleared submissions from 1989 to 1997.
Browse the FDA 510(k) cleared devices submitted by North American Sterilization & Packaging Co. Filter by specialty or product code using the sidebar.
16 devices
Cleared
Mar 10, 1997
NASP HYDROCOLLOID DRESSING (REGULAR OR THIN)
General & Plastic Surgery
138d
Cleared
Nov 29, 1996
NASP TRANSPARENT DRESSING
General & Plastic Surgery
72d
Cleared
Aug 02, 1996
HYDROGEL SKIN DRESSING
General & Plastic Surgery
45d
Cleared
Dec 03, 1993
NORTEC STER SALINE-O.9% SODIUM CHLOR FOR DEV IRRI
General & Plastic Surgery
393d
Cleared
Dec 03, 1993
NORTEC STERILE WATER FOR DEVICE IRRIGATION
General & Plastic Surgery
393d
Cleared
Jul 21, 1993
NORTEC STERILE WATER FOR CATHETER BALLOON INFLATIO
Gastroenterology & Urology
281d
Cleared
Nov 01, 1991
NORTEC CONNECTING TUBE SET
General Hospital
189d
Cleared
Sep 23, 1991
NORTEC ROBERTAZZI NASOPHARYNGEAL AIRWAY
Anesthesiology
154d
Cleared
Aug 15, 1991
NORTEC URETERAL STENT
Gastroenterology & Urology
177d
Cleared
Dec 18, 1990
CONTROL-TIP CYSTOSCOPIC ELECTRODES
Gastroenterology & Urology
153d
Cleared
Dec 18, 1990
FLEXIBLE ENDOSCOPIC ELECTRODES
Gastroenterology & Urology
153d
Cleared
Sep 20, 1990
STERILE INSTRUMENT DRAPE
General Hospital
87d