ClearanceBrief
510(k) K983647 ยท MJG Device, Percutaneous, Biopsy

ECHO-COAT ULTRASOUND NEEDLES

ApplicantSts Biopolymers, Rockville MD, US
DecisionSubstantially Equivalent, Jan 20, 1999
ReceivedOct 16, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K983647

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.