ClearanceBrief
510(k) K092387 ยท FEB Accessories, Cleaning, For Endoscope

MEDIVATORS DSD EDGE ENDOSCOPE REPROCESSING SYSTEM

ApplicantMinntech Corp., Minneapolis MN, US
DecisionSubstantially Equivalent, Apr 5, 2010
ReceivedAug 5, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K092387

DateFirm and productCodeLinked 510(k)
Aug 8, 2024Steris Corporation
Hookup Model/Catalog Number: DSD-110-HU0163 Product Description: Hookups provide the interface between DSD Automated Endoscope Reprocessors ( AER ) and endoscopes, which allow perfusion of liquids di
Open, Classified
FEBNone listed

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