510(k) K962149 ยท FMI Needle, Hypodermic, Single Lumen
SAFETY CRADLE
| Applicant | Specialized Health Products, Inc., Sandy UT, US |
| Decision | Substantially Equivalent, Oct 11, 1996 |
| Received | Jun 4, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962149
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.