Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Alliance Medical, Inc.

FDA 510(k) & PMA Approved Devices — 11 products

Total Devices11
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K051438 VANGUARD REPROCESSED COMPRESSION GARMENTS (HILL-ROM)JOW2006-04-04 View
510(k) K050518 REPROCESSED PHACOEMUISIFICATION TIPSNKX2005-09-23 View
510(k) K030187 REPROCESSED ELECTROPHYSIOLOGY CATHETERNLH2003-09-24 View
510(k) K021654 REPROCESSED COMPRESSION SLEEVEJOW2003-02-05 View
510(k) K012634 REPROCESSED EXTERNAL FIXATION DEVICEKTW2002-06-24 View
510(k) K012630 REPROCESSED LINVATEC ARTHROSCOPIC BURSHRX2001-11-09 View
510(k) K012613 REPROCSSED LINVATEC SHAVERSHRX2001-11-07 View
510(k) K012611 REPROCESSED DYONICS ARTHROSCOPIC SHAVERSHRX2001-11-07 View
510(k) K990198 AMIB7IYO1999-06-29 View
510(k) K951976 ECHO. AKHOIYO1996-07-26 View
510(k) K931091 DISPOSABLE AMA STERILE DRAPE SHEET, CAT. NO. 5252KKX1994-02-03 View
↑