ClearanceBrief
510(k) K790851 ยท KOH Instrument, Manual, General Obstetric-Gynecologic

VAGI-PRESS #401

ApplicantC. Intl., Mchenry IL, US
DecisionSubstantially Equivalent, Jul 30, 1979
ReceivedMay 4, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K790851

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.