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Catheter Technology Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
13
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K880571CATH-TECH PORT IMPLANTABLE VASCULAR ACCESS SYSTEMMarch 4, 1988
K871080PERIPHERALLY INSERTED CENTRAL VENOUS CATHETERAugust 12, 1987
K871998GROSHONG CV CATHETER REPAIR KITJune 24, 1987
K860256BRAWN AND GROSHONG CATHETERSMarch 28, 1986
K842577CATH-TECH POLYURETHANE UMBILICAL VESSMarch 13, 1985
K842147CATH-TECH CHOLANGIOGRAPHY CATHETEROctober 2, 1984
K840339UMBILICAL VESSEL CATHETERJuly 25, 1984
K831386GROSHONG CATHETER, LONG TERM TYPEOctober 14, 1983
K831365TESTCORP ANAJune 2, 1983
K831361BETA-PREGJune 2, 1983
K831366TESTCORP PREGJune 2, 1983
K831362TESTCORP CRPMay 27, 1983
K831363TESTCORP ASOMay 16, 1983