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Phoenix Biomedical Corp.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K033017PHOENIX INFUSION CATHETERApril 7, 2004
K030468ACURA ELITE GRAVITY COMPENSATING RESERVOIROctober 15, 2003
K024101PHOENIX UNIVERSAL SHUNT SYSTEMJanuary 27, 2003
K024040ACCURA ELITE SHUNT SYSTEMJanuary 27, 2003
K021644PERF (OMMAYA STYLE) RESERVOIRSAugust 6, 2002
K002476LUMBOPERITONEAL SHUNT SYSTEMNovember 9, 2000
K000514RUMBAR DRAINAGE SYSTEMMay 10, 2000
K991429DIAMOND II VALVEMay 19, 1999
K990256CRX WORLD SHUNTApril 1, 1999
K974096CRX DIAMOND VALVEDecember 8, 1998
K962144PHOENIX ETE TISSUE EXTENSION SYSTEMJanuary 14, 1997
K960435PHOENIX CRX VALVEAugust 27, 1996
K953128SUTURE CORDFebruary 9, 1996