ClearanceBrief
510(k) K193330 ยท PYT Device, Fertility Diagnostic, Contraceptive, Software Application

Clue Birth Control

ApplicantBiowink GmbH, Berlin, DE
DecisionSubstantially Equivalent, Feb 18, 2021
ReceivedDec 2, 2019
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K193330

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.