ClearanceBrief
510(k) K833256 ยท HOY Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)

CROUCH CORNEAL PROTECTOR

ApplicantStar Instrument Co., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 8, 1984
ReceivedSep 20, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K833256

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.