510(k) K850485 ยท JQC Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use
ROTOR SYSTEMS A/S-400 & LA/S-400
| Applicant | E.I. Dupont DE Nemours & Co., Inc., Wilmington DE, US |
| Decision | Substantially Equivalent, Mar 12, 1985 |
| Received | Feb 7, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850485
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.