510(k) K000085 ยท FMI Needle, Hypodermic, Single Lumen
PORTSETT
| Applicant | Portsett, Inc., Rancho Santa Margarita CA, US |
| Decision | Substantially Equivalent, Mar 17, 2000 |
| Received | Jan 12, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000085
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.