ClearanceBrief
510(k) K213669 ยท GEX Powered Laser Surgical Instrument

LIGHTSCALPEL LS-4020

ApplicantLightscalpel, Inc., Bothell WA, US
DecisionSubstantially Equivalent, Feb 15, 2023
ReceivedNov 22, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K213669

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.