FDA 510(k)

Dozee VS

Número K: K221555 · 2022-12-15

RequerenteTurtle Shell Technologies Private Limited

Data da decisão2022-12-15

Código do produtoBZQ

Comité consultivoAN

DecisãoSubstantially Equivalent

Resumo do dispositivo

Dozee VS is the device name listed in this FDA 510(k) record. The listed applicant is Turtle Shell Technologies Private Limited. It received FDA 510(k) clearance on 2022-12-15 under 510(k) number K221555. The device is classified under product code BZQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Dozee VS?

Dozee VS is a medical device that received FDA 510(k) clearance on 2022-12-15. The listed applicant is Turtle Shell Technologies Private Limited. The 510(k) number is K221555.

When did Dozee VS receive FDA 510(k) clearance?

Dozee VS received FDA 510(k) clearance on 2022-12-15, under 510(k) number K221555.

Who is the listed applicant for Dozee VS?

The FDA 510(k) record lists Turtle Shell Technologies Private Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Dozee VS?

The FDA product code for Dozee VS is BZQ.

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