The following data is part of a premarket notification filed by Diatech, Inc. with the FDA for Dia Thrombin Dia Plastin.
| Device ID | K840802 |
| 510k Number | K840802 |
| Device Name: | DIA THROMBIN DIA PLASTIN |
| Classification | Test, Time, Prothrombin |
| Applicant | DIATECH, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GJS |
| CFR Regulation Number | 864.7750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-02-23 |
| Decision Date | 1984-05-01 |