Guardian Angel Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Guardian Angel Products, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Guardian Angel Products, Inc. has 5 FDA 510(k) cleared medical devices. Based in Huntingdon Valley, US.
Historical record: 5 cleared submissions from 1990 to 2003. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Guardian Angel Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Guardian Angel Products, Inc.
5 devices
Cleared
Jul 11, 2003
MODIFICATION TO ZAP GUARD DEFIBRILLATOR TEST PROBE
Cardiovascular
141d
Cleared
Jul 13, 1993
NEEDLE-GRABBER
General & Plastic Surgery
347d
Cleared
Jul 09, 1993
THE ELEVENTH FINGER
General & Plastic Surgery
343d
Cleared
Oct 11, 1991
GUARDIAN GEL, SURGEON'S GLOVING CREAM
General Hospital
234d
Cleared
Jul 31, 1990
ZAP-GUARD
Cardiovascular
230d