ClearanceBrief
510(k) K901881 ยท LNN

VIBROMETRY SYSTEM

ApplicantBruel & Kjaer Instruments, Inc., Hoffman Estates IL, US
DecisionSubstantially Equivalent, May 31, 1991
ReceivedApr 26, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K901881

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.