ClearanceBrief
510(k) K900894 ยท GCQ Endoscope, Flexible

MEDILASE SERIES 2100 ENDOSCOPE

ApplicantMedical Laser, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, Jun 22, 1990
ReceivedFeb 27, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K900894

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.