Atlas FDA

Sun Biomedical Laboratories, Inc.

3 FDA 510(k) clearances · Recalling firm

Sort:Newest firstOldest first

◉ Watch Sun Biomedical Laboratories, Inc.

RecordFirmDate
VisuaLine Single Dip Oxycodone; intended for in vitro immunoassay test completed by visual recall (Z-1873-2008)Sun Biomedical Laboratories, Inc.2008-09-17
VisuaLine Propoxyphene; Propoxyphene test system, intended for in vitro immunoassay test c recall (Z-1874-2008)Sun Biomedical Laboratories, Inc.2008-09-17
VisuaLine Tricyclic Antidepressants: Six Dip (COC-THC-OPI-MET-BZD-OXD); Six Dip (COC-THC-O recall (Z-1875-2008)Sun Biomedical Laboratories, Inc.2008-09-17

Track Sun Biomedical Laboratories, Inc. automatically

Every clearance here is in the API, with alerts when new ones post.