ClearanceBrief
510(k) K852154 ยท

ACKRAD SIALOGRAPHY CATHETER

ApplicantAckrad Laboratories, Cranford NJ, US
DecisionSubstantially Equivalent, Jun 26, 1985
ReceivedMay 17, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K852154

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.