ClearanceBrief
510(k) K895779 ยท CBK Ventilator, Continuous, Facility Use

MODIFIED PERMCATH TRAY (2ND SUBMISSION)

ApplicantQuinton, Inc., Seattle WA, US
DecisionSubstantially Equivalent, Dec 7, 1989
ReceivedSep 7, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K895779

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.