The following data is part of a premarket notification filed by Technam, Inc. with the FDA for H-i-m-test For Detecting Human Chor. Gon.
| Device ID | K800055 |
| 510k Number | K800055 |
| Device Name: | H-I-M-TEST FOR DETECTING HUMAN CHOR. GON |
| Classification | Agglutination Method, Human Chorionic Gonadotropin |
| Applicant | TECHNAM, INC. 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 | 1980-01-10 |
| Decision Date | 1980-01-29 |