ClearanceBrief
510(k) K884696 ยท HDR Cap, Cervical

RESUBMITTED ARTIFICIAL INSEMINATION INSTRUMENT SET

ApplicantLaboratoire Ccd C/O Washington Regulatory Services, Ringoes NJ, US
DecisionSubstantially Equivalent, Jan 27, 1989
ReceivedNov 9, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K884696

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.