ClearanceBrief
510(k) K820533 ยท GIE Fibrometer

B4182-1

ApplicantAmerican Scientific Products, Mchenry IL, US
DecisionSubstantially Equivalent, Apr 8, 1982
ReceivedMar 2, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K820533

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.