ClearanceBrief
510(k) K030394 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection

FLUID SAMPLE RETRIEVAL SYSTEM

ApplicantBiomed Personal Metabolic and Nutritional Testing, Memphis TN, US
DecisionSubstantially Equivalent, Oct 27, 2003
ReceivedFeb 5, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K030394

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.