ClearanceBrief
510(k) K924725 ยท MDM Instrument, Manual, Surgical, General Use

AMERICAN BIOMED, INC. MICROSURGICAL INSTRUMENTS

ApplicantAmerican Biomaterials Corp., The Woodlands TX, US
DecisionSubstantially Equivalent, Feb 5, 1993
ReceivedSep 21, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K924725

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.