ClearanceBrief
510(k) K895100 ยท ITX Transducer, Ultrasonic, Diagnostic

ECHO GEL (RAINFOREST)

ApplicantLead-Lok, Inc., Sandpoint ID, US
DecisionSubstantially Equivalent, Nov 3, 1989
ReceivedAug 15, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K895100

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.