The following data is part of a premarket notification filed by Hospira, Inc. with the FDA for Hospira Mednet Medication Management Suite.
| Device ID | K141102 |
| 510k Number | K141102 |
| Device Name: | HOSPIRA MEDNET MEDICATION MANAGEMENT SUITE |
| Classification | Pump, Infusion |
| Applicant | HOSPIRA, INC. 275 NORTH FIELD DR. Lake Forest, IL 60045 |
| Contact | Tom Gutierrez |
| Correspondent | Tom Gutierrez HOSPIRA, INC. 275 NORTH FIELD DR. Lake Forest, IL 60045 |
| Product Code | FRN |
| CFR Regulation Number | 880.5725 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-04-29 |
| Decision Date | 2014-07-08 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10887787009139 | K141102 | 000 |
| 10887787009115 | K141102 | 000 |
| 10887709101811 | K141102 | 000 |