FDA 510(k)

CONDUIT Lateral Switch Plate

Número K: K221325 · 2022-08-25

Data da decisão2022-08-25

Código do produtoMAX

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

CONDUIT Lateral Switch Plate is the device name listed in this FDA 510(k) record. The listed applicant is Medos International SARL. It received FDA 510(k) clearance on 2022-08-25 under 510(k) number K221325. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the CONDUIT Lateral Switch Plate?

CONDUIT Lateral Switch Plate is a medical device that received FDA 510(k) clearance on 2022-08-25. The listed applicant is Medos International SARL. The 510(k) number is K221325.

When did CONDUIT Lateral Switch Plate receive FDA 510(k) clearance?

CONDUIT Lateral Switch Plate received FDA 510(k) clearance on 2022-08-25, under 510(k) number K221325.

Who is the listed applicant for CONDUIT Lateral Switch Plate?

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

What is the FDA product code for CONDUIT Lateral Switch Plate?

The FDA product code for CONDUIT Lateral Switch Plate is MAX.

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Fonte oficial

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