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FDA 510(k)

CRX DIAMOND VALVE

K-Number: K974096 · 1998-12-08

ApplicantPhoenix Biomedical Corp.
Decision Date1998-12-08
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CRX DIAMOND 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 1998-12-08 under 510(k) number K974096. 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 CRX DIAMOND VALVE?

CRX DIAMOND VALVE is a medical device that received FDA 510(k) clearance on 1998-12-08. The listed applicant is Phoenix Biomedical Corp.. The 510(k) number is K974096.

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

CRX DIAMOND VALVE received FDA 510(k) clearance on 1998-12-08, under 510(k) number K974096.

Who is the listed applicant for CRX DIAMOND 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 CRX DIAMOND VALVE?

The FDA product code for CRX DIAMOND 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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