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FDA 510(k)

HIRSCH BIPOLAR COAGULATION FORCEPS AND ADAPTOR CABLES

K-Number: K942319 · 1994-06-08

ApplicantBerchtold Holding GmbH
Decision Date1994-06-08
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HIRSCH BIPOLAR COAGULATION FORCEPS AND ADAPTOR CABLES is the device name listed in this FDA 510(k) record. The listed applicant is Berchtold Holding GmbH. It received FDA 510(k) clearance on 1994-06-08 under 510(k) number K942319. 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 HIRSCH BIPOLAR COAGULATION FORCEPS AND ADAPTOR CABLES?

HIRSCH BIPOLAR COAGULATION FORCEPS AND ADAPTOR CABLES is a medical device that received FDA 510(k) clearance on 1994-06-08. The listed applicant is Berchtold Holding GmbH. The 510(k) number is K942319.

When did HIRSCH BIPOLAR COAGULATION FORCEPS AND ADAPTOR CABLES receive FDA 510(k) clearance?

HIRSCH BIPOLAR COAGULATION FORCEPS AND ADAPTOR CABLES received FDA 510(k) clearance on 1994-06-08, under 510(k) number K942319.

Who is the listed applicant for HIRSCH BIPOLAR COAGULATION FORCEPS AND ADAPTOR CABLES?

The FDA 510(k) record lists Berchtold Holding GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HIRSCH BIPOLAR COAGULATION FORCEPS AND ADAPTOR CABLES?

The FDA product code for HIRSCH BIPOLAR COAGULATION FORCEPS AND ADAPTOR CABLES is GEI.

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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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