ClearanceBrief
510(k) K781767 ยท KOH Instrument, Manual, General Obstetric-Gynecologic

INSTRUMENT CURNETT MINI-CONER BIOPSY

ApplicantC.R. Bard, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Dec 7, 1978
ReceivedOct 16, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K781767

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.