510(k) K883749 ยท JQW Station, Pipetting And Diluting, For Clinical Use
PROBE(TM) MODELS 700 AND 1000
| Applicant | Packard Instrument Co., Inc., Downers Grove IL, US |
| Decision | Substantially Equivalent, Nov 10, 1988 |
| Received | Sep 1, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883749
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.