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FDA 510(k)

RADIONICS LUMBOPERITONEAL SHUNT

K-Number: K000057 · 2000-03-20

ApplicantRadionics, Inc.
Decision Date2000-03-20
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

RADIONICS LUMBOPERITONEAL SHUNT is the device name listed in this FDA 510(k) record. The listed applicant is Radionics, Inc.. It received FDA 510(k) clearance on 2000-03-20 under 510(k) number K000057. 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 RADIONICS LUMBOPERITONEAL SHUNT?

RADIONICS LUMBOPERITONEAL SHUNT is a medical device that received FDA 510(k) clearance on 2000-03-20. The listed applicant is Radionics, Inc.. The 510(k) number is K000057.

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

RADIONICS LUMBOPERITONEAL SHUNT received FDA 510(k) clearance on 2000-03-20, under 510(k) number K000057.

Who is the listed applicant for RADIONICS LUMBOPERITONEAL SHUNT?

The FDA 510(k) record lists Radionics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RADIONICS LUMBOPERITONEAL SHUNT?

The FDA product code for RADIONICS LUMBOPERITONEAL SHUNT is 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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