ClearanceBrief
510(k) K882384 ยท LRX Case, Contact Lens

DELUXE CONTACT LENS HOLDER (HARD & SOFT) #283

ApplicantMagnivision, Inc., Miami FL, US
DecisionSubstantially Equivalent, Jun 23, 1989
ReceivedJun 9, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K882384

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.