510(k) K932889 ยท FMI Needle, Hypodermic, Single Lumen
PERRY SPECIALTIES DESIGNS NEEDLE GUARD
| Applicant | Perry Specialties Design, Inc., Columbus IN, US |
| Decision | Substantially Equivalent, May 28, 1996 |
| Received | Jun 14, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932889
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.