510(k) K020229 ยท JPK Mixture, Hematology Quality Control
R & D BODY FLUID CONTROL
| Applicant | R&D Systems, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Feb 6, 2002 |
| Received | Jan 23, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020229
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.