510(k) K970800 ยท FPA Set, Administration, Intravascular
MAXCESS NEEDLEFREE - Y- SITE (100713)
| Applicant | Solopak Medical Products, Inc., Elk Grove Village IL, US |
| Decision | Substantially Equivalent, Apr 2, 1997 |
| Received | Mar 4, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970800
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.