510(k) K980558 ยท MEB Pump, Infusion, Elastomeric
PAINBUSTER INFUSION SYSTEM
| Applicant | I-Flow Corp., Lake Forest CA, US |
| Decision | Substantially Equivalent, May 28, 1998 |
| Received | Feb 13, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980558
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.