510(k) K001690 ยท FMI Needle, Hypodermic, Single Lumen
PROTECTIV SAFETY BLOOD COLLECTION NEEDLE
| Applicant | Johnson & Johnson Medical, Inc., Arlington TX, US |
| Decision | Substantially Equivalent, Jul 31, 2000 |
| Received | Jun 2, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001690
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.