Hpi, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Hpi, Inc. has 6 FDA 510(k) cleared medical devices. Based in Newton Centre, US.
Historical record: 6 cleared submissions from 1990 to 1993. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Hpi, Inc. Filter by specialty or product code using the sidebar.
6 devices
Cleared
Feb 08, 1993
POWDER FREE NITRILE GLOVE
General Hospital
333d
Cleared
Jun 17, 1992
HPI BROWN NITRILE SENSI-GRIP SURGICAL GLOVES
General Hospital
218d
Cleared
Mar 20, 1991
HPI SENSI-SHIELD GLOVE KIT
General Hospital
49d
Cleared
Mar 07, 1991
SENSI RADS LEAD LATEX RADIATION PROT. GLOVE, STER.
Radiology
128d
Cleared
Dec 03, 1990
HPI TRI-RADS VINYL RADIATION PROTECTION GLOVES
Radiology
19d
Cleared
Apr 20, 1990
HPI POWDER FREE NON-STERILE EXAMINATION GLOVES
General Hospital
14d