FDA 510(k)

Dozee VS

N.º K: K221555 · 2022-12-15

SolicitanteTurtle Shell Technologies Private Limited

Fecha de decisión2022-12-15

Código de productoBZQ

Comité asesorAN

DecisiónSubstantially Equivalent

Resumen del 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.

Preguntas frecuentes

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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Fuente oficial

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