FDA 510(k)

Clue Birth Control

Numéro K : K193330 · 2021-02-18

Date de décision2021-02-18

Code produitPYT

Comité consultatifOB

DécisionSubstantially Equivalent

Résumé du dispositif

Clue Birth Control is the device name listed in this FDA 510(k) record. The listed applicant is Biowink GmbH. It received FDA 510(k) clearance on 2021-02-18 under 510(k) number K193330. The device is classified under product code PYT. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

What is the Clue Birth Control?

Clue Birth Control is a medical device that received FDA 510(k) clearance on 2021-02-18. The listed applicant is Biowink GmbH. The 510(k) number is K193330.

When did Clue Birth Control receive FDA 510(k) clearance?

Clue Birth Control received FDA 510(k) clearance on 2021-02-18, under 510(k) number K193330.

Who is the listed applicant for Clue Birth Control?

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

What is the FDA product code for Clue Birth Control?

The FDA product code for Clue Birth Control is PYT.

Essais cliniques associés

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Dispositifs connexes (Code : PYT)

K253694Natural CyclesNatural Cycles Nordic AB K250561Natural CyclesNatural Cycles Nordic AB K241006Natural CyclesNatural Cycles Nordic AB K231274Natural CyclesNatural Cycles Nordic AB K202897Natural CyclesNatural Cycles Nordic AB

Source officielle

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