The following data is part of a premarket notification filed by Universal Reagents, Inc. with the FDA for Universal Reagent Factor Viii Deficient Plasma.
| Device ID | K970593 |
| 510k Number | K970593 |
| Device Name: | UNIVERSAL REAGENT FACTOR VIII DEFICIENT PLASMA |
| Classification | Plasma, Coagulation Factor Deficient |
| Applicant | UNIVERSAL REAGENTS, INC. 2858 N. PENNSYLVANIA ST. Indianapolis, IN 46205 |
| Contact | Jorge Miller |
| Correspondent | Jorge Miller UNIVERSAL REAGENTS, INC. 2858 N. PENNSYLVANIA ST. Indianapolis, IN 46205 |
| Product Code | GJT |
| CFR Regulation Number | 864.7290 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-02-18 |
| Decision Date | 1997-04-25 |
| Summary: | summary |