FDA 510(k)

EndoGator Endoscopy Irrigation Tubing

Número K: K220395 · 2022-03-11

Data da decisão2022-03-11

Código do produtoFEQ

Comité consultivoGU

DecisãoSubstantially Equivalent

Resumo do dispositivo

EndoGator Endoscopy Irrigation Tubing is the device name listed in this FDA 510(k) record. The listed applicant is STERIS Corporation. It received FDA 510(k) clearance on 2022-03-11 under 510(k) number K220395. The device is classified under product code FEQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the EndoGator Endoscopy Irrigation Tubing?

EndoGator Endoscopy Irrigation Tubing is a medical device that received FDA 510(k) clearance on 2022-03-11. The listed applicant is STERIS Corporation. The 510(k) number is K220395.

When did EndoGator Endoscopy Irrigation Tubing receive FDA 510(k) clearance?

EndoGator Endoscopy Irrigation Tubing received FDA 510(k) clearance on 2022-03-11, under 510(k) number K220395.

Who is the listed applicant for EndoGator Endoscopy Irrigation Tubing?

The FDA 510(k) record lists STERIS Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EndoGator Endoscopy Irrigation Tubing?

The FDA product code for EndoGator Endoscopy Irrigation Tubing is FEQ.

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Fonte oficial

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