ClearanceBrief
510(k) K023238 ยท JOM Plethysmograph, Photoelectric, Pneumatic Or Hydraulic

MCPULSE

ApplicantMeridian Co., Ltd., Deer Field IL, US
DecisionSubstantially Equivalent, Feb 19, 2003
ReceivedSep 27, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K023238

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.