H & P Industries, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
H & P Industries, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
H & P Industries, Inc. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1983 to 1990. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by H & P Industries, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - H & P Industries, Inc.
5 devices
Cleared
Jun 22, 1990
TRIA-SONIC ULTRA SOUND TRANSMISSION GEL
General & Plastic Surgery
101d
Cleared
Apr 01, 1987
LUBRICATING JELLY
General Hospital
8d
Cleared
Apr 09, 1986
GAMMA RADIATION STERILIZED ALCOHOL PREP PADS
General Hospital
27d
Cleared
Apr 06, 1983
PROVIDONE-IODINE SWABSTICKS
General & Plastic Surgery
58d
Cleared
Apr 06, 1983
PROVIDONE-IODINE PREP-PADS & TOWELETTES
General & Plastic Surgery
58d