510(k) K071088 ยท FMI Needle, Hypodermic, Single Lumen
LIFE LATCH SHARPS & BIOHAZARD CONTAINER
| Applicant | M&M Industries, Inc., Potomac MD, US |
| Decision | Substantially Equivalent, Jul 5, 2007 |
| Received | Apr 18, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071088
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.