Phoenix Biomedical Corp.
Phoenix Biomedical Corp. holds FDA 510(k) medical device clearances, first cleared 1996, most recent 2003.
Top product codes for Phoenix Biomedical Corp.
Recent clearances by Phoenix Biomedical Corp.
- K030468 — ACURA ELITE GRAVITY COMPENSATING RESERVOIR
- K024040 — ACCURA ELITE SHUNT SYSTEM
- K024101 — PHOENIX UNIVERSAL SHUNT SYSTEM
- K021644 — PERF (OMMAYA STYLE) RESERVOIRS
- K002476 — LUMBOPERITONEAL SHUNT SYSTEM
- K000514 — RUMBAR DRAINAGE SYSTEM
- K991429 — DIAMOND II VALVE
- K990256 — CRX WORLD SHUNT
- K974096 — CRX DIAMOND VALVE
- K962144 — PHOENIX ETE TISSUE EXTENSION SYSTEM
- K960435 — PHOENIX CRX VALVE
- K953128 — SUTURE CORD
Data sourced from openFDA. This site is unofficial and independent of the FDA.