ClearanceBrief
510(k) K900308 ยท HDR Cap, Cervical

SPERM SELECT SYSTEM

ApplicantPharmacia, Inc., Piscataway NJ, US
DecisionSubstantially Equivalent, Apr 13, 1990
ReceivedJan 22, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K900308

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.