ClearanceBrief
510(k) K770332 ยท JOM Plethysmograph, Photoelectric, Pneumatic Or Hydraulic

AMPLIFIER, PHOTOPULSE, MODEL PA13

ApplicantMedsonics, Mchenry IL, US
DecisionSubstantially Equivalent, Feb 24, 1977
ReceivedFeb 17, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K770332

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.