ClearanceBrief
510(k) K800834 ยท KOH Instrument, Manual, General Obstetric-Gynecologic

SER-TEX

ApplicantV.S.S.I., Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jun 30, 1980
ReceivedApr 14, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K800834

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.