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FDA 510(k)

LUMBOPERITONEAL SHUNT SYSTEM

K-Number: K002476 · 2000-11-09

ApplicantPhoenix Biomedical Corp.
Decision Date2000-11-09
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

LUMBOPERITONEAL SHUNT SYSTEM 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 2000-11-09 under 510(k) number K002476. 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 LUMBOPERITONEAL SHUNT SYSTEM?

LUMBOPERITONEAL SHUNT SYSTEM is a medical device that received FDA 510(k) clearance on 2000-11-09. The listed applicant is Phoenix Biomedical Corp.. The 510(k) number is K002476.

When did LUMBOPERITONEAL SHUNT SYSTEM receive FDA 510(k) clearance?

LUMBOPERITONEAL SHUNT SYSTEM received FDA 510(k) clearance on 2000-11-09, under 510(k) number K002476.

Who is the listed applicant for LUMBOPERITONEAL SHUNT SYSTEM?

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 LUMBOPERITONEAL SHUNT SYSTEM?

The FDA product code for LUMBOPERITONEAL SHUNT SYSTEM 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) RESERVOIRSK000514RUMBAR DRAINAGE SYSTEMK991429DIAMOND II VALVE

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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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