ClearanceBrief
510(k) K213569 ยท GEX Powered Laser Surgical Instrument

HOLLYWOOD SPECTRA Laser System

ApplicantLutronic Corporation, Deogyang-Gu, Goyang-Si, KR
DecisionSubstantially Equivalent, Feb 4, 2022
ReceivedNov 9, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K213569

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.