North American Medical Products, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
North American Medical Products, Inc. has 6 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 6 cleared submissions from 1984 to 2001.
Browse the FDA 510(k) cleared devices submitted by North American Medical Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - North American Medical Products, Inc.
6 devices
Cleared
Feb 02, 2001
SAFE-POINT VAC, SAFE-POINT M-D BLOOD COLLECTION SYSTEMS
General Hospital
219d
Cleared
Feb 12, 1991
SAFE-SITE NEEDLE COVER
General Hospital
76d
Cleared
Mar 27, 1990
PORT-O-SCOPE(TM)
Ear, Nose, Throat
168d
Cleared
Nov 27, 1989
D.L. SCOPE OPHTHALMOSCOPE
Ophthalmic
39d
Cleared
Aug 08, 1986
D.L. SCOPE(R) OTOSCOPE
Ear, Nose, Throat
25d
Cleared
May 23, 1984
D.L. SCOPE BLADE & HANDLE
Anesthesiology
23d