ClearanceBrief
510(k) K940405 ยท KMI Monitor, Bed Patient

TELETOM

ApplicantBerchtold Holding GmbH, Tuttlingen, DE
DecisionSubstantially Equivalent, Apr 14, 1994
ReceivedJan 27, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K940405

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.