510(k) K933848 ยท FPA Set, Administration, Intravascular
PRESPO 7, SELF-SUFFICIENT DRIP DEVICE
| Applicant | Bonding Corp., Coraopolis PA, US |
| Decision | Substantially Equivalent, Mar 3, 1995 |
| Received | Aug 6, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933848
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.