510(k) K033039 ยท MEB Pump, Infusion, Elastomeric
MODIFICATION TO: ACCUFUSER, ACCUFUSER PLUS, STANDARD PROCEDURE KITS
| Applicant | Mckinley, Inc., Wheat Ridge CO, US |
| Decision | Substantially Equivalent, Oct 7, 2003 |
| Received | Sep 29, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K033039
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.