510(k) K900579 ยท JJQ Colorimeter, Photometer, Spectrophotometer For Clinical Use
AUTOREADER CALIBRATION TEST PLATE
| Applicant | Bio-Tek Instruments, Inc., Winooski VT, US |
| Decision | Substantially Equivalent, Feb 27, 1990 |
| Received | Feb 7, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900579
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.