ClearanceBrief
510(k) K090587 ยท OAN Orthosis, Cranial, Laser Scan

STARLIGHT

ApplicantOrthomerica Products, Inc., Orlando FL, US
DecisionSubstantially Equivalent, Jul 17, 2009
ReceivedMar 4, 2009
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K090587

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.