FDA 510(k)

INTRACEPT FLEXIBLE BI-POLAR RF PROBE AND CURVED INSTRUMENT SET, MODELS: FG0018, FG0026

K-Number: K083856 · 2009-01-22

Decision Date2009-01-22

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

INTRACEPT FLEXIBLE BI-POLAR RF PROBE AND CURVED INSTRUMENT SET, MODELS: FG0018, FG0026 is the device name listed in this FDA 510(k) record. The listed applicant is Relievant Medsystems, Inc.. It received FDA 510(k) clearance on 2009-01-22 under 510(k) number K083856. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTRACEPT FLEXIBLE BI-POLAR RF PROBE AND CURVED INSTRUMENT SET, MODELS: FG0018, FG0026?

INTRACEPT FLEXIBLE BI-POLAR RF PROBE AND CURVED INSTRUMENT SET, MODELS: FG0018, FG0026 is a medical device that received FDA 510(k) clearance on 2009-01-22. The listed applicant is Relievant Medsystems, Inc.. The 510(k) number is K083856.

When did INTRACEPT FLEXIBLE BI-POLAR RF PROBE AND CURVED INSTRUMENT SET, MODELS: FG0018, FG0026 receive FDA 510(k) clearance?

INTRACEPT FLEXIBLE BI-POLAR RF PROBE AND CURVED INSTRUMENT SET, MODELS: FG0018, FG0026 received FDA 510(k) clearance on 2009-01-22, under 510(k) number K083856.

Who is the listed applicant for INTRACEPT FLEXIBLE BI-POLAR RF PROBE AND CURVED INSTRUMENT SET, MODELS: FG0018, FG0026?

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

What is the FDA product code for INTRACEPT FLEXIBLE BI-POLAR RF PROBE AND CURVED INSTRUMENT SET, MODELS: FG0018, FG0026?

The FDA product code for INTRACEPT FLEXIBLE BI-POLAR RF PROBE AND CURVED INSTRUMENT SET, MODELS: FG0018, FG0026 is GEI.

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Official Source

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