510(k) K010328 ยท PJE Blood/Plasma Collection Device For Dna Testing
MULTIPLE (IZON DNA BLOOD COLLECTION KIT)
| Applicant | Izon Business Products, Inc., West Nyack NY, US |
| Decision | Substantially Equivalent, Apr 9, 2001 |
| Received | Feb 2, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010328
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.