ClearanceBrief
510(k) K952625 ยท JPA System, Multipurpose For In Vitro Coagulation Studies

COAGUCHEK SYSTEM

ApplicantBoehringer Mannheim Corp., Indianapolis IN, US
DecisionSubstantially Equivalent, Nov 21, 1995
ReceivedJun 8, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K952625

DateFirm and productCodeLinked 510(k)
Oct 28, 2005Roche Diagnostics Corp.
Roche CoaguChek System Controls; Catalog number 7745, Part numbers 054207608 and 04393201001.
Terminated
GJSNone listed

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