ClearanceBrief
510(k) K780761 ยท JOM Plethysmograph, Photoelectric, Pneumatic Or Hydraulic

ELECTRO-PLETHYSMOGRAPH

ApplicantBiotecx Laboratories, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jun 30, 1978
ReceivedMay 9, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K780761

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.