ClearanceBrief
510(k) K863702 ยท JOM Plethysmograph, Photoelectric, Pneumatic Or Hydraulic

PULSE CUFF RECORDER MODEL PCR100

ApplicantImex Medical Systems, Inc., Golden CO, US
DecisionSubstantially Equivalent, Jun 12, 1987
ReceivedSep 23, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K863702

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.