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FDA 510(k)

INTRACEPT BI-POLAR RF PROBE, MODEL 04814

K-Number: K070443 · 2007-10-05

ApplicantRelievant Medsystems, Inc.
Decision Date2007-10-05
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

INTRACEPT BI-POLAR RF PROBE, MODEL 04814 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 2007-10-05 under 510(k) number K070443. 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 BI-POLAR RF PROBE, MODEL 04814?

INTRACEPT BI-POLAR RF PROBE, MODEL 04814 is a medical device that received FDA 510(k) clearance on 2007-10-05. The listed applicant is Relievant Medsystems, Inc.. The 510(k) number is K070443.

When did INTRACEPT BI-POLAR RF PROBE, MODEL 04814 receive FDA 510(k) clearance?

INTRACEPT BI-POLAR RF PROBE, MODEL 04814 received FDA 510(k) clearance on 2007-10-05, under 510(k) number K070443.

Who is the listed applicant for INTRACEPT BI-POLAR RF PROBE, MODEL 04814?

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 BI-POLAR RF PROBE, MODEL 04814?

The FDA product code for INTRACEPT BI-POLAR RF PROBE, MODEL 04814 is GEI.

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Other records listing Relievant Medsystems, Inc. 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.

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Related Devices (Code: 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.

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