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FDA 510(k)

GENICON BIPOLAR FORCEPS MODEL # 600-005-005

K-Number: K041968 · 2004-11-03

ApplicantGenicon
Decision Date2004-11-03
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

GENICON BIPOLAR FORCEPS MODEL # 600-005-005 is the device name listed in this FDA 510(k) record. The listed applicant is Genicon. It received FDA 510(k) clearance on 2004-11-03 under 510(k) number K041968. 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 GENICON BIPOLAR FORCEPS MODEL # 600-005-005?

GENICON BIPOLAR FORCEPS MODEL # 600-005-005 is a medical device that received FDA 510(k) clearance on 2004-11-03. The listed applicant is Genicon. The 510(k) number is K041968.

When did GENICON BIPOLAR FORCEPS MODEL # 600-005-005 receive FDA 510(k) clearance?

GENICON BIPOLAR FORCEPS MODEL # 600-005-005 received FDA 510(k) clearance on 2004-11-03, under 510(k) number K041968.

Who is the listed applicant for GENICON BIPOLAR FORCEPS MODEL # 600-005-005?

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

What is the FDA product code for GENICON BIPOLAR FORCEPS MODEL # 600-005-005?

The FDA product code for GENICON BIPOLAR FORCEPS MODEL # 600-005-005 is GEI.

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Other records listing Genicon 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.

K100090IMPLANTABLE CLIPK061417GENICON DISPOSABLE ELECTROSURGICAL INSTRUMENTATION, MODEL 533-005-910K041967GENICON SUCTION IRRIGATION SYSTEM

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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