FDA 510(k)

Supra Non-Stick Bipolar Forceps

Número K: K213042 · 2022-11-17

RequerenteGuenter Bissinger Medizintechnik GmbH

Data da decisão2022-11-17

Código do produtoGEI

Comité consultivoSU

DecisãoSubstantially Equivalent

Resumo do dispositivo

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.

Perguntas frequentes

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.

Ensaios clínicos relacionados

Registros relacionados são pareados automaticamente usando nomes, códigos de produtos ou outros metadados. Um pareamento não estabelece um vínculo clínico, científico, corporativo ou regulatório verificado; revise as fontes oficiais vinculadas.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Dispositivos Relacionados (Código: GEI)

K254196HARMONIC 1100 Shears (HAR1120); HARMONIC 1100 Shears (HAR1136)Ethicon Endo-Surgery, LLC K261959Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Push Button Switch (0703-046-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Push Button Switch, Bulk Non-Sterile (0703-046-102);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Rocker Switch (0703-047-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Rocker Switch, Bulk Non-Sterile (0703-047-102)Stryker Instruments K261070LigaSure™ RAS Maryland Jaw Vessel Sealer/Divider, Nano-coatedCovidien, LLC K254185Potenza PrimeJeisys Medical Incorporated K262364Ellian Enigma RF DeviceEllian Corp K253859Scarlet Pro (Scarlet Pro)VIOL Co., Ltd.

Fonte oficial

Ver na base de dados da FDA →

Dados provenientes da FDA Open API. Para informações mais recentes e oficiais, consulte sempre o registro oficial.