ClearanceBrief
510(k) K973850 ยท HFO Recorder, Pressure, Intrauterine

ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY #M007

ApplicantAlexander Mfg. Co., Mason City IA, US
DecisionSubstantially Equivalent, Nov 12, 1997
ReceivedOct 8, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K973850

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.