ClearanceBrief
510(k) K945320 ยท ITX Transducer, Ultrasonic, Diagnostic

TETRAD MODEL BG22, AUTOMATIC BIOPSY UNIT MODEL

ApplicantTetra Corp., Englewood CO, US
DecisionSubstantially Equivalent, May 11, 1995
ReceivedNov 1, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K945320

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.