FDA 510(k)

WebCeph

Número K: K220903 · 2022-08-17

Data da decisão2022-08-17

Código do produtoLLZ

Comité consultivoRA

DecisãoSubstantially Equivalent

Resumo do dispositivo

WebCeph is the device name listed in this FDA 510(k) record. The listed applicant is Assemblecircle Corp.. It received FDA 510(k) clearance on 2022-08-17 under 510(k) number K220903. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the WebCeph?

WebCeph is a medical device that received FDA 510(k) clearance on 2022-08-17. The listed applicant is Assemblecircle Corp.. The 510(k) number is K220903.

When did WebCeph receive FDA 510(k) clearance?

WebCeph received FDA 510(k) clearance on 2022-08-17, under 510(k) number K220903.

Who is the listed applicant for WebCeph?

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

What is the FDA product code for WebCeph?

The FDA product code for WebCeph is LLZ.

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