ClearanceBrief
510(k) K780257 ยท HOZ Sponge, Ophthalmic

MICROSPEARS

ApplicantSparta Instrument Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 23, 1978
ReceivedFeb 15, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K780257

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.