The following data is part of a premarket notification filed by Texas Immunology, Inc. with the FDA for V-trend Beta-hcg Dry-spot Test.
| Device ID | K875262 |
| 510k Number | K875262 |
| Device Name: | V-TREND BETA-HCG DRY-SPOT TEST |
| Classification | Agglutination Method, Human Chorionic Gonadotropin |
| Applicant | TEXAS IMMUNOLOGY, INC. 5400 SPUR 248 Tyler, TX 75707 |
| Contact | Charles W Gill |
| Correspondent | Charles W Gill TEXAS IMMUNOLOGY, INC. 5400 SPUR 248 Tyler, TX 75707 |
| Product Code | JHJ |
| CFR Regulation Number | 862.1155 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-12-22 |
| Decision Date | 1988-02-02 |