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FDA 510(k) Applications Submitted by PHOENIX BIOMEDICAL CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K990256
01/27/1999
CRX WORLD SHUNT
PHOENIX BIOMEDICAL CORP.
K030468
02/12/2003
ACURA ELITE GRAVITY COMPENSATING RESERVOIR
PHOENIX BIOMEDICAL CORP.
K000514
02/16/2000
RUMBAR DRAINAGE SYSTEM
PHOENIX BIOMEDICAL CORP.
K991429
04/26/1999
DIAMOND II VALVE
PHOENIX BIOMEDICAL CORP.
K021644
05/20/2002
PERF (OMMAYA STYLE) RESERVOIRS
PHOENIX BIOMEDICAL CORP.
K002476
08/11/2000
LUMBOPERITONEAL SHUNT SYSTEM
PHOENIX BIOMEDICAL CORP.
K024040
12/06/2002
ACCURA ELITE SHUNT SYSTEM
PHOENIX BIOMEDICAL CORP.
K024101
12/12/2002
PHOENIX UNIVERSAL SHUNT SYSTEM
PHOENIX BIOMEDICAL CORP.
K974096
10/30/1997
CRX DIAMOND VALVE
PHOENIX BIOMEDICAL CORP.
K960435
01/31/1996
PHOENIX CRX VALVE
PHOENIX BIOMEDICAL CORP.
K962144
06/03/1996
PHOENIX ETE TISSUE EXTENSION SYSTEM
PHOENIX BIOMEDICAL CORP.
K953128
07/06/1995
SUTURE CORD
PHOENIX BIOMEDICAL CORP.
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