ClearanceBrief
510(k) K873848 ยท GDM Needle, Aspiration And Injection, Reusable

RETROBULBAR NEEDLE

ApplicantHealthtek, Inc., Nevada City CA, US
DecisionSubstantially Equivalent, Oct 23, 1987
ReceivedSep 22, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K873848

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.