ClearanceBrief
510(k) K884098 ยท BYI Percussor, Powered-Electric

THAIRAPY(TM) BRONCHIAL DRAINAGE SYSTEM, MODEL 101

ApplicantAmerican Biosystems, Inc., Marine On St. Croix MN, US
DecisionSubstantially Equivalent, Dec 16, 1988
ReceivedSep 28, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K884098

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.