Adroit Medical Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Adroit Medical Systems, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Adroit Medical Systems, Inc. has 6 FDA 510(k) cleared medical devices. Based in Morganton, US.
Historical record: 6 cleared submissions from 1992 to 2008.
Browse the FDA 510(k) cleared devices submitted by Adroit Medical Systems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Adroit Medical Systems, Inc.
6 devices
Cleared
Jun 06, 2008
SOFT AIR, MODEL SA 4000 AND MISTRAL AIR, MODEL MA0100
Cardiovascular
158d
Cleared
Jan 29, 1998
SAFEPASS STERILIZATION POUCH
General Hospital
101d
Cleared
Sep 10, 1997
HTP-1500 LOCALIZED HEAT THERAPY PUMP
Physical Medicine
232d
Cleared
Jan 10, 1997
STERILE SOFT-TEMP
Physical Medicine
162d
Cleared
Dec 11, 1992
SOFT-TEMP
Cardiovascular
232d
Cleared
Nov 06, 1992
SOFT-COVER
General Hospital
196d