ClearanceBrief
510(k) K983220 ยท FAT Bougie, Esophageal, And Gastrointestinal, Gastro-Urology

STRYKER INFRAVISION ESOPHAGEAL KIT

ApplicantStryker Endoscopy, Santa Clara CA, US
DecisionSubstantially Equivalent, Jun 4, 1999
ReceivedSep 14, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K983220

DateFirm and productCodeLinked 510(k)
Feb 1, 2011Stryker Endoscopy
Stryker Endoscopy, Infravision Esophageal Kit, Model Numbers: 220180548, 220180540, 220180560
Terminated
FATNone listed
Dec 28, 2010Stryker Endoscopy
Stryker Infravision Esophageal Kit, Model Numbers 220180548, 220180540, 220180560, manufactured by Stryker Endoscopy San Jose.
Terminated
FATNone listed

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