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 Corp.

FDA 510(k) & PMA Approved Devices — 36 products

Total Devices36
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K060648 REPROCESSED PHACOEMULSIFICATION TIPSNKX2007-03-19 View
510(k) K061045 REPROCESSED ELECTROPHYSIOLOGY CATHETERSNLH2006-08-31 View
510(k) K060049 REPROCESSED COMPRESSION SLEEVESJOW2006-02-24 View
510(k) K060091 ALLIANCE MEDICAL CORPORATION REPROCESSED COMPRESSION SLEEVESJOW2006-02-17 View
510(k) K053316 REPROCESSED COMPRESSION SLEEVESJOW2006-02-13 View
510(k) K052918 REPROCESSED EXTERNAL FIXATION DEVICESKTT2006-01-27 View
510(k) K052603 REPROCESSED DAIG LIVEWIRE ELECTROPHYSIOLOGY CATHETERSNLH2005-11-16 View
510(k) K052414 REPROCESSED ELECTROPHYSIOLOGY CATHETERNLH2005-11-16 View
510(k) K052064 ALLIANCE MEDICAL CORPORATION REPROCESSED EXTERNAL FIXATION DEVICESKTT2005-08-25 View
510(k) K052062 ALLIANCE MEDICAL CORPORATION REPROCESSED EXTERNAL FIXATION DEVICESKTT2005-08-25 View
510(k) K052065 ALLIANCE MEDICAL CORPORATION REPROCESSED EXTERNAL FIXATION DEVICESKTT2005-08-22 View
510(k) K051554 ALLIANCE MEDICAL CORPORATION REPROCESSED EXTERNAL FIXATION DEVICESKTT2005-06-29 View
510(k) K043358 REPROCESSED ULTRASONIC SCALPELSNLQ2005-06-06 View
510(k) K043392 REPROCESSED ELECTROPHYSIOLOGY CATHETERSNLH2005-03-25 View
510(k) K043393 REPROCESSED EP TECHNOLOGIES ELECTROPHYSIOLOGY CATHETERSNLH2005-03-23 View
510(k) K033436 REPROCESSED DIAGNOSTIC ULTRASOUND CATHETEROWQ2005-03-16 View
510(k) K041978 REPROCESSED DIAMOND BURSNLN2004-11-23 View
510(k) K030279 REPROCESSED ELECTROPHYSIOLOGY CATHETERNLH2003-10-03 View
510(k) K030109 ELECTROPHYSIOLOGY CATHETERNLH2003-08-08 View
510(k) K032058 MODIFICATION TO REPROCESSED SYNTHES EXTERNAL FIXATION DEVICESKTT2003-07-30 View
↑