Axiom Medical, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
28
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K993592AXIOM MULTIPURPOSE WOUND DRAINMay 17, 2000
K971851INTERPLEURAL ANESTHESIA CATHETERJanuary 22, 1998
K965146FLAT CLOSED WOUND DRAIN WITH TROCARMarch 10, 1997
K934895GLASSMAN SILICONE CATHETEROctober 13, 1994
K922760ATRAUM WOUND DRESSING--MODIFICATIONOctober 30, 1992
K905422PVC ROUND WOUND DRAINSFebruary 11, 1991
K904218SUCTION SYSTEMOctober 31, 1990
K904133DISPOSABLE FLUID COLLECTION BAGOctober 11, 1990
K863247AXIOM TROCAR THORACIC CATHETERAugust 29, 1986
K861306SUCTION SYSTEMJune 9, 1986
K852614ATRAUM WOUND DRESSINGAugust 30, 1985
K852241AXIOM ATRAUM TROCAR CATHETERJune 14, 1985
K841574QUAZAR ESOPHAGEAL STETHOSCOPEAugust 15, 1984
K842084AXIOM FEMORAL VENUS CATHETERAugust 1, 1984
K841593AXIOM THORACIC CATHETERSJune 5, 1984
K832476SILICONE SOFT-PAK EPISTAXIS CATHETERNovember 3, 1983
K832416AXIOM HYDROMER WOUND DRAINSOctober 31, 1983
K832475AXIOM PERFUSSION CANNULAOctober 19, 1983
K831823AXIOM FEEDING GASTRO TUBEAugust 12, 1983
K820161AXIOM LIG-A-BOOTSMarch 15, 1982