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FDA 510(k)

SELECT-SUTTER MICRO BIPOLAR FORCEPS

K-Number: K992760 · 1999-10-25

ApplicantSelect Medizintechnik Hermann Sutter GmbH
Decision Date1999-10-25
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SELECT-SUTTER MICRO BIPOLAR FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Select Medizintechnik Hermann Sutter GmbH. It received FDA 510(k) clearance on 1999-10-25 under 510(k) number K992760. 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 SELECT-SUTTER MICRO BIPOLAR FORCEPS?

SELECT-SUTTER MICRO BIPOLAR FORCEPS is a medical device that received FDA 510(k) clearance on 1999-10-25. The listed applicant is Select Medizintechnik Hermann Sutter GmbH. The 510(k) number is K992760.

When did SELECT-SUTTER MICRO BIPOLAR FORCEPS receive FDA 510(k) clearance?

SELECT-SUTTER MICRO BIPOLAR FORCEPS received FDA 510(k) clearance on 1999-10-25, under 510(k) number K992760.

Who is the listed applicant for SELECT-SUTTER MICRO BIPOLAR FORCEPS?

The FDA 510(k) record lists Select Medizintechnik Hermann Sutter GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SELECT-SUTTER MICRO BIPOLAR FORCEPS?

The FDA product code for SELECT-SUTTER MICRO BIPOLAR FORCEPS is GEI.

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Official Source

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