ClearanceBrief
510(k) K953710 ยท JJQ Colorimeter, Photometer, Spectrophotometer For Clinical Use

ELX808 AUTOMATED MICROPLATE READERS

ApplicantBio-Tek Instruments, Inc., Winooski VT, US
DecisionSubstantially Equivalent, Oct 25, 1995
ReceivedAug 9, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K953710

DateFirm and productCodeLinked 510(k)
Mar 8, 2005Roche Diagnostics Corp.
BioTek brand Automated Microplate Reader; model ELx808, Roche catalog number 03145387001.
Terminated
JJQNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.