The following data is part of a premarket notification filed by Health Diagnostics Corp. with the FDA for In-home Early Pregnancy Test Kit.
| Device ID | K802334 |
| 510k Number | K802334 |
| Device Name: | IN-HOME EARLY PREGNANCY TEST KIT |
| Classification | Agglutination Method, Human Chorionic Gonadotropin |
| Applicant | HEALTH DIAGNOSTICS CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JHJ |
| CFR Regulation Number | 862.1155 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-09-23 |
| Decision Date | 1980-10-10 |