ClearanceBrief
510(k) K052690 ยท NUJ Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed

SURETEK REPROCESSED LAPAROSCOPIC INSTRUMENTS

ApplicantSuretek Medical, Greenville SC, US
DecisionSubstantially Equivalent, May 12, 2006
ReceivedSep 28, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K052690

No recall in the FDA data names this 510(k).

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