The following data is part of a premarket notification filed by Amico Lab, Inc. with the FDA for Anti-herpes Simplex Virus Type 1 Or 2.
| Device ID | K842663 |
| 510k Number | K842663 |
| Device Name: | ANTI-HERPES SIMPLEX VIRUS TYPE 1 OR 2 |
| Classification | Antisera, Cf, Herpesvirus Hominis 1,2 |
| Applicant | AMICO LAB, INC. TN 37209 - |
| Product Code | GQO |
| CFR Regulation Number | 866.3305 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-07-10 |
| Decision Date | 1985-12-06 |