ClearanceBrief
510(k) K023173 ยท MDM Instrument, Manual, Surgical, General Use

ANDREWS INTRODUCER, MODEL ASI01

ApplicantAndrews Surgical Innovations, Ltd., Co. Dublin, IE
DecisionSubstantially Equivalent, Dec 18, 2002
ReceivedSep 23, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K023173

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.