ClearanceBrief
510(k) K970824 ยท JOY Device, Automated Cell-Locating

MDX 2000, DIGITAL ANALYZER

ApplicantShotwell & Carr, Inc., Dallas TX, US
DecisionSubstantially Equivalent, May 30, 1997
ReceivedMar 6, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K970824

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.