ClearanceBrief
510(k) K790682 ยท

TONOTEST BLOOD PRESSURE DEVICE

ApplicantRobert Bosch Corp., Mchenry IL, US
DecisionUnknown, Apr 11, 1979
ReceivedApr 11, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K790682

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.