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FDA 510(k)

TECNO REUSABLE, ELECTROSURGICAL, BIPOLAR FORCEPS

K-Number: K964176 · 1997-08-14

ApplicantTecno Instruments (Usa), Inc.
Decision Date1997-08-14
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TECNO REUSABLE, ELECTROSURGICAL, BIPOLAR FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Tecno Instruments (Usa), Inc.. It received FDA 510(k) clearance on 1997-08-14 under 510(k) number K964176. 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 TECNO REUSABLE, ELECTROSURGICAL, BIPOLAR FORCEPS?

TECNO REUSABLE, ELECTROSURGICAL, BIPOLAR FORCEPS is a medical device that received FDA 510(k) clearance on 1997-08-14. The listed applicant is Tecno Instruments (Usa), Inc.. The 510(k) number is K964176.

When did TECNO REUSABLE, ELECTROSURGICAL, BIPOLAR FORCEPS receive FDA 510(k) clearance?

TECNO REUSABLE, ELECTROSURGICAL, BIPOLAR FORCEPS received FDA 510(k) clearance on 1997-08-14, under 510(k) number K964176.

Who is the listed applicant for TECNO REUSABLE, ELECTROSURGICAL, BIPOLAR FORCEPS?

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

What is the FDA product code for TECNO REUSABLE, ELECTROSURGICAL, BIPOLAR FORCEPS?

The FDA product code for TECNO REUSABLE, ELECTROSURGICAL, BIPOLAR FORCEPS 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.

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