ClearanceBrief
Company ยท US

Phoenix Biomedical Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1996 to 2004. Name variants (Inc, Corp, punctuation) are merged.

13510(k) clearances (0 in 12 months)
1recalls (0 in 12 months)
1recalls that name a 510(k)

Product codes

CodeDeviceRecords
JXGShunt, Central Nervous System And Components12
GASSuture, Nonabsorbable, Synthetic, Polyester1
MKYSystem, Skin Closure1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Apr 7, 2004K033017PHOENIX INFUSION CATHETER
Phoenix Biomedical
JXG
Oct 15, 2003K030468ACURA ELITE GRAVITY COMPENSATING RESERVOIR
Phoenix Biomedical Corp.
JXG
Jan 27, 2003K024101PHOENIX UNIVERSAL SHUNT SYSTEM
Phoenix Biomedical Corp.
JXG
Jan 27, 2003K024040ACCURA ELITE SHUNT SYSTEM
Phoenix Biomedical Corp.
JXG
Aug 6, 2002K021644PERF (OMMAYA STYLE) RESERVOIRS
Phoenix Biomedical Corp.
JXG
Nov 9, 2000K002476LUMBOPERITONEAL SHUNT SYSTEM
Phoenix Biomedical Corp.
JXG
May 10, 2000K000514RUMBAR DRAINAGE SYSTEM
Phoenix Biomedical Corp.
JXG
May 19, 1999K991429DIAMOND II VALVE
Phoenix Biomedical Corp.
JXG
Apr 1, 1999K990256CRX WORLD SHUNT
Phoenix Biomedical Corp.
JXG
Dec 8, 1998K974096CRX DIAMOND VALVE
Phoenix Biomedical Corp.
JXG
Jan 14, 1997K962144PHOENIX ETE TISSUE EXTENSION SYSTEM
Phoenix Biomedical Corp.
MKY
Aug 27, 1996K960435PHOENIX CRX VALVE
Phoenix Biomedical Corp.
JXG
Feb 9, 1996K953128SUTURE CORD
Phoenix Biomedical Corp.
GAS

Latest recalls

DateFirm and productCodeLinked 510(k)
Jul 20, 2004Phoenix Biomedical
Cruciform Slit Valve
Terminated
JXGK790126
K853363
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