The following data is part of a premarket notification filed by Armkel, Llc. with the FDA for Answer (r).
| Device ID | K812924 |
| 510k Number | K812924 |
| Device Name: | ANSWER (R) |
| Classification | Agglutination Method, Human Chorionic Gonadotropin |
| Applicant | ARMKEL, LLC. 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 | 1981-10-19 |
| Decision Date | 1981-11-02 |