510(k) K901162 ยท FMI Needle, Hypodermic, Single Lumen
STERIMATIC(TM) SAFETY NEEDLE
| Applicant | Sterimatic Worldwide, Ltd., Stroud, Gloucestershire, GB |
| Decision | Substantially Equivalent, Sep 28, 1990 |
| Received | Mar 13, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901162
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.