ClearanceBrief
510(k) K951204 ยท GEX Powered Laser Surgical Instrument

SHARPLAN MODEL 712 ACUSPOT MICROMANIPULATOR

ApplicantSharplan Lasers, Inc., Allendale NJ, US
DecisionSubstantially Equivalent, Jun 1, 1995
ReceivedMar 17, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K951204

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.