ClearanceBrief
510(k) K970530 ยท GEY Motor, Surgical Instrument, Ac-Powered

ANSPACH LUBRICATING SYSTEM II

ApplicantThe Anspach Effort, Inc., Palm Beach Gardens FL, US
DecisionSubstantially Equivalent, May 5, 1997
ReceivedFeb 12, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K970530

DateFirm and productCodeLinked 510(k)
Jun 25, 2014The Anspach Effort, Inc.
ANSPACH***REF-98-0056***Custom Device Autolube III modified with a swivel***Rx Only*** This device is intended to be used with Anspach Systems
Terminated
GEYNone listed

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