The following data is part of a premarket notification filed by Omni Intl., Inc. with the FDA for Omnimed I.v. Solution Admin. Set.
| Device ID | K853255 |
| 510k Number | K853255 |
| Device Name: | OMNIMED I.V. SOLUTION ADMIN. SET |
| Classification | Set, Administration, Intravascular |
| Applicant | OMNI INTL., INC. 870 RESEARCH DR. UNIT 5 Palm Springs, CA 92263 |
| Contact | Raman Kadevari |
| Correspondent | Raman Kadevari OMNI INTL., INC. 870 RESEARCH DR. UNIT 5 Palm Springs, CA 92263 |
| Product Code | FPA |
| CFR Regulation Number | 880.5440 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-08-02 |
| Decision Date | 1985-08-23 |