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Concord Laboratories, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
42
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K883840DRI-VENT ARTERIAL BLOOD SAMPLING KITMay 16, 1989
K871825MECONIUM SUCTION CATHETERJune 29, 1987
K864535TRACHEOBRONCHIAL SUCTION CATHETER, CAT. NO. 6110January 6, 1987
K862039CONCORD CARE TRAYJuly 3, 1986
K854601SPRING GUIDE CATHETER ANESTHESIA CONDUCTION CATHJanuary 10, 1986
K854327SUBCUTANEOUS TUNNELING NEEDLES & HANDLESNovember 13, 1985
K851134REGIONAL ANESTHESIA TRAYSJuly 15, 1985
K842095EPIDURAL TRAYSJuly 3, 1984
K841486ARTERIAL BLOOD SAMPLING KITSMay 23, 1984
K840987VAPORIZED HEPARINApril 5, 1984
K840986PREFILLED PULSATOR SYRINGEApril 5, 1984
K840709MID-STREAM URINE COLLECTION SETSApril 3, 1984
K833814SANI CATCH BAMarch 19, 1984
K840988NO POUR BASINMarch 7, 1984
K833993ALCOHOL SWABSJanuary 30, 1984
K833936ACETONE ALCOHOL SWABSJanuary 30, 1984
K833582PULSATOR ARTERIAL BLOOD SAMPLING SYRINDecember 27, 1983
K832778EPIDURAL SYRINGESeptember 26, 1983
K811009PREFILLED PULSATOR SYRINGEJune 12, 1981
K810995PREFILLED PULSATOR SYRINGEMay 21, 1981