510(k) K992072 ยท FPA Set, Administration, Intravascular
BOLUS ACCESSORY SET
| Applicant | I-Flow Corp., Lake Forest CA, US |
| Decision | Substantially Equivalent, Sep 15, 1999 |
| Received | Jun 19, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992072
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.