ClearanceBrief
510(k) K841299 ยท GDM Needle, Aspiration And Injection, Reusable

BIERMAN BIOPSY NEEDLE

ApplicantPopper & Sons, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, May 2, 1984
ReceivedMar 30, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K841299

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.