ClearanceBrief
510(k) K952220 ยท LYR Helicobacter Pylori

MERETEK BREATH TEST FOR H.PYLORI COLLECTION KIT

ApplicantMeretek Diagnostics, Inc., Houston TX, US
DecisionSubstantially Equivalent, Sep 17, 1996
ReceivedMay 11, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K952220

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.