The following data is part of a premarket notification filed by Hospira, Inc. with the FDA for Hospira Mednet Medication Management Suite.
| Device ID | K042609 |
| 510k Number | K042609 |
| Device Name: | HOSPIRA MEDNET MEDICATION MANAGEMENT SUITE |
| Classification | Pump, Infusion |
| Applicant | HOSPIRA, INC. 275 N. FIELD DRIVE Lake Forest, IL 60045 -5045 |
| Contact | Ray Silkaitis |
| Product Code | FRN |
| CFR Regulation Number | 880.5725 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2004-09-24 |
| Decision Date | 2004-10-06 |
| Summary: | summary |