Phoenix Biomedical Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Phoenix Biomedical Corp. - FDA 510(k) Cleared Devices
12
Total
11
Cleared
0
Denied
Phoenix Biomedical Corp. has 11 FDA 510(k) cleared neurology devices. Based in Valley Forge, US.
Historical record: 11 cleared submissions from 1996 to 2003.
Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Phoenix Biomedical Corp.
12 devices
Cleared
Oct 15, 2003
ACURA ELITE GRAVITY COMPENSATING RESERVOIR
Neurology
245d
Cleared
Jan 27, 2003
ACCURA ELITE SHUNT SYSTEM
Neurology
52d
Cleared
Jan 27, 2003
PHOENIX UNIVERSAL SHUNT SYSTEM
Neurology
46d
Cleared
Aug 06, 2002
PERF (OMMAYA STYLE) RESERVOIRS
Neurology
78d
Cleared
Nov 09, 2000
LUMBOPERITONEAL SHUNT SYSTEM
Neurology
90d
Cleared
May 10, 2000
RUMBAR DRAINAGE SYSTEM
Neurology
84d
Cleared
May 19, 1999
DIAMOND II VALVE
Neurology
23d
Cleared
Apr 01, 1999
CRX WORLD SHUNT
Neurology
64d
Cleared
Dec 08, 1998
CRX DIAMOND VALVE
Neurology
404d
Cleared
Jan 14, 1997
PHOENIX ETE TISSUE EXTENSION SYSTEM
General & Plastic Surgery
225d
Cleared
Aug 27, 1996
PHOENIX CRX VALVE
Neurology
209d
Cleared
Feb 09, 1996
SUTURE CORD
General & Plastic Surgery
218d