FDA 510(k)

Supra Non-Stick Bipolar Forceps

Numéro K : K213042 · 2022-11-17

DemandeurGuenter Bissinger Medizintechnik GmbH

Date de décision2022-11-17

Code produitGEI

Comité consultatifSU

DécisionSubstantially Equivalent

Résumé du dispositif

Supra Non-Stick Bipolar Forceps is the device name listed in this FDA 510(k) record. The listed applicant is Guenter Bissinger Medizintechnik GmbH. It received FDA 510(k) clearance on 2022-11-17 under 510(k) number K213042. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

What is the Supra Non-Stick Bipolar Forceps?

Supra Non-Stick Bipolar Forceps is a medical device that received FDA 510(k) clearance on 2022-11-17. The listed applicant is Guenter Bissinger Medizintechnik GmbH. The 510(k) number is K213042.

When did Supra Non-Stick Bipolar Forceps receive FDA 510(k) clearance?

Supra Non-Stick Bipolar Forceps received FDA 510(k) clearance on 2022-11-17, under 510(k) number K213042.

Who is the listed applicant for Supra Non-Stick Bipolar Forceps?

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

What is the FDA product code for Supra Non-Stick Bipolar Forceps?

The FDA product code for Supra Non-Stick Bipolar Forceps is GEI.

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Source officielle

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