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FDA 510(k)

CRX WORLD SHUNT

K-Number: K990256 · 1999-04-01

ApplicantPhoenix Biomedical Corp.
Decision Date1999-04-01
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CRX WORLD SHUNT 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 1999-04-01 under 510(k) number K990256. 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 WORLD SHUNT?

CRX WORLD SHUNT is a medical device that received FDA 510(k) clearance on 1999-04-01. The listed applicant is Phoenix Biomedical Corp.. The 510(k) number is K990256.

When did CRX WORLD SHUNT receive FDA 510(k) clearance?

CRX WORLD SHUNT received FDA 510(k) clearance on 1999-04-01, under 510(k) number K990256.

Who is the listed applicant for CRX WORLD SHUNT?

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 WORLD SHUNT?

The FDA product code for CRX WORLD SHUNT 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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