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FDA 510(k)

PHOENIX CRX VALVE

K-Number: K960435 · 1996-08-27

ApplicantPhoenix Biomedical Corp.
Decision Date1996-08-27
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

PHOENIX CRX VALVE is the device name listed in this FDA 510(k) record. The listed applicant is Phoenix Biomedical Corp.. It received FDA 510(k) clearance on 1996-08-27 under 510(k) number K960435. The device is classified under product code JXG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHOENIX CRX VALVE?

PHOENIX CRX VALVE is a medical device that received FDA 510(k) clearance on 1996-08-27. The listed applicant is Phoenix Biomedical Corp.. The 510(k) number is K960435.

When did PHOENIX CRX VALVE receive FDA 510(k) clearance?

PHOENIX CRX VALVE received FDA 510(k) clearance on 1996-08-27, under 510(k) number K960435.

Who is the listed applicant for PHOENIX CRX VALVE?

The FDA 510(k) record lists Phoenix Biomedical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PHOENIX CRX VALVE?

The FDA product code for PHOENIX CRX VALVE is JXG.

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Other records listing Phoenix Biomedical Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K030468ACURA ELITE GRAVITY COMPENSATING RESERVOIRK024101PHOENIX UNIVERSAL SHUNT SYSTEMK024040ACCURA ELITE SHUNT SYSTEMK021644PERF (OMMAYA STYLE) RESERVOIRSK002476LUMBOPERITONEAL SHUNT SYSTEMK000514RUMBAR DRAINAGE SYSTEM

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Related Devices (Code: JXG)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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