ClearanceBrief
510(k) K882404 ยท PCF Sampler, Endocervical

KEVOR-CURETTE

ApplicantEuro-Med Intl., Alameda CA, US
DecisionSubstantially Equivalent, Jul 8, 1988
ReceivedJun 10, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K882404

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.