ClearanceBrief
510(k) K900380 ยท FET Endoscopic Video Imaging System/Component, Gastroenterology-Urology

MEDILASE 5010 ENDOSCOPE CONSOLE

ApplicantMedical Laser, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, May 15, 1990
ReceivedJan 26, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K900380

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.