FDA 510(k)

SURGI-LINK BIPOLAR MICRO FORCEPS

K-Number: K946246 · 1995-03-07

Decision Date1995-03-07

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

SURGI-LINK BIPOLAR MICRO FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Unimed Surgical Products, Inc.. It received FDA 510(k) clearance on 1995-03-07 under 510(k) number K946246. 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 SURGI-LINK BIPOLAR MICRO FORCEPS?

SURGI-LINK BIPOLAR MICRO FORCEPS is a medical device that received FDA 510(k) clearance on 1995-03-07. The listed applicant is Unimed Surgical Products, Inc.. The 510(k) number is K946246.

When did SURGI-LINK BIPOLAR MICRO FORCEPS receive FDA 510(k) clearance?

SURGI-LINK BIPOLAR MICRO FORCEPS received FDA 510(k) clearance on 1995-03-07, under 510(k) number K946246.

Who is the listed applicant for SURGI-LINK BIPOLAR MICRO FORCEPS?

The FDA 510(k) record lists Unimed Surgical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURGI-LINK BIPOLAR MICRO FORCEPS?

The FDA product code for SURGI-LINK BIPOLAR MICRO FORCEPS is GEI.

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Other records listing Unimed Surgical Products, Inc. as applicant

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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.