The following data is part of a premarket notification filed by Orion Life Systems, Inc. with the FDA for Sterile I.v. Start Kit.
| Device ID | K902810 |
| 510k Number | K902810 |
| Device Name: | STERILE I.V. START KIT |
| Classification | Set, Administration, Intravascular |
| Applicant | ORION LIFE SYSTEMS, INC. 124 MESSNER DR. Wheeling, IL 60090 |
| Contact | John L Laemmar |
| Correspondent | John L Laemmar ORION LIFE SYSTEMS, INC. 124 MESSNER DR. Wheeling, IL 60090 |
| Product Code | FPA |
| CFR Regulation Number | 880.5440 [🔎] |
| Decision | Substantially Equivalent - Kit With Drugs (SEKD) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-06-27 |
| Decision Date | 1990-11-13 |