ClearanceBrief
510(k) K890380 ยท HFB Forceps, Biopsy, Gynecological

CERVICAL BIOPSY FORCEPS

ApplicantKinetic Medical Products, Erie PA, US
DecisionSubstantially Equivalent, Feb 27, 1989
ReceivedJan 23, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K890380

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.