The following data is part of a premarket notification filed by Hospira, Inc. with the FDA for Hospira Administration Sets.
| Device ID | K160870 |
| 510k Number | K160870 |
| Device Name: | Hospira Administration Sets |
| Classification | Set, Administration, Intravascular |
| Applicant | HOSPIRA, INC. 375 FIELD DRIVE Lake Forest, IL 60045 |
| Contact | David Blonski |
| Correspondent | David Blonski HOSPIRA, INC. 375 FIELD DRIVE Lake Forest, IL 60045 |
| Product Code | FPA |
| CFR Regulation Number | 880.5440 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-03-30 |
| Decision Date | 2016-06-01 |
| Summary: | summary |