FDA 510(k)

HOOK ELECTRODE, NEEDLE ELECTRODE, COAGULATION BUTTON ELECTRODE

K-Number: K973341 · 1997-11-13

ApplicantRichard Wolf Medical Instruments Corp.

Decision Date1997-11-13

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

HOOK ELECTRODE, NEEDLE ELECTRODE, COAGULATION BUTTON ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corp.. It received FDA 510(k) clearance on 1997-11-13 under 510(k) number K973341. 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 HOOK ELECTRODE, NEEDLE ELECTRODE, COAGULATION BUTTON ELECTRODE?

HOOK ELECTRODE, NEEDLE ELECTRODE, COAGULATION BUTTON ELECTRODE is a medical device that received FDA 510(k) clearance on 1997-11-13. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K973341.

When did HOOK ELECTRODE, NEEDLE ELECTRODE, COAGULATION BUTTON ELECTRODE receive FDA 510(k) clearance?

HOOK ELECTRODE, NEEDLE ELECTRODE, COAGULATION BUTTON ELECTRODE received FDA 510(k) clearance on 1997-11-13, under 510(k) number K973341.

Who is the listed applicant for HOOK ELECTRODE, NEEDLE ELECTRODE, COAGULATION BUTTON ELECTRODE?

The FDA 510(k) record lists Richard Wolf Medical Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HOOK ELECTRODE, NEEDLE ELECTRODE, COAGULATION BUTTON ELECTRODE?

The FDA product code for HOOK ELECTRODE, NEEDLE ELECTRODE, COAGULATION BUTTON ELECTRODE 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.