ClearanceBrief
510(k) K980547 ยท GEX Powered Laser Surgical Instrument

NIDEK PRIMA MODEL GYC-1500/2000

ApplicantNidek, Inc., Fremont CA, US
DecisionSubstantially Equivalent, May 13, 1998
ReceivedFeb 12, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K980547

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.