Alliance Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Alliance Medical, Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Alliance Medical, Inc. has 11 FDA 510(k) cleared medical devices. Based in Santa Ynez, US.
Historical record: 11 cleared submissions from 1994 to 2006.
Browse the FDA 510(k) cleared devices submitted by Alliance Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Alliance Medical, Inc.
11 devices
Cleared
Apr 04, 2006
VANGUARD REPROCESSED COMPRESSION GARMENTS (HILL-ROM)
Cardiovascular
307d
Cleared
Sep 23, 2005
REPROCESSED PHACOEMUISIFICATION TIPS
Ophthalmic
206d
Cleared
Sep 24, 2003
REPROCESSED ELECTROPHYSIOLOGY CATHETER
Cardiovascular
246d
Cleared
Feb 05, 2003
REPROCESSED COMPRESSION SLEEVE
Cardiovascular
261d
Cleared
Jun 24, 2002
REPROCESSED EXTERNAL FIXATION DEVICE
Orthopedic
315d
Cleared
Nov 09, 2001
REPROCESSED LINVATEC ARTHROSCOPIC BURS
Orthopedic
88d
Cleared
Nov 07, 2001
REPROCESSED DYONICS ARTHROSCOPIC SHAVERS
Orthopedic
86d
Cleared
Nov 07, 2001
REPROCSSED LINVATEC SHAVERS
Orthopedic
86d
Cleared
Jun 29, 1999
AMIB7
Radiology
159d
Cleared
Jul 26, 1996
ECHO. AKHO
Radiology
456d
Cleared
Feb 03, 1994
DISPOSABLE AMA STERILE DRAPE SHEET, CAT. NO. 5252
General Hospital
337d