ClearanceBrief
510(k) K933611 ยท ISD Exerciser, Measuring

THE BTE WS30

ApplicantBaltimore Therapeutic Equipment Co., Hanover MD, US
DecisionSubstantially Equivalent, Jun 20, 1994
ReceivedJul 19, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K933611

DateFirm and productCodeLinked 510(k)
Jul 6, 2015BTE Technologies, Inc.
Primus (THE BTE WS30), model PrimusRS (PRRS) and Primus+ (PR30) a measuring exercise equipment device designed to provide active and passive torque resistance to patient motion during rehabilitation t
Terminated
ISDNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.