Submission Details
| 510(k) Number | K842531 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | June 28, 1984 |
| Decision Date | December 06, 1985 |
| Days to Decision | 526 days |
| Submission Type | Traditional |
| Review Panel | Immunology (IM) |
| Summary | — |
K842531 is an FDA 510(k) clearance for the AMIZYME-HSV TYPES 1 & 2 TEST KITS. This device is classified as a Antisera, Cf, Herpesvirus Hominis 1,2 (Class II — Special Controls, product code GQO).
Submitted by Amico Lab, Inc.. The FDA issued a Cleared decision on December 6, 1985, 526 days after receiving the submission on June 28, 1984.
This device falls under the Immunology FDA review panel. Regulated under 21 CFR 866.3305.
| 510(k) Number | K842531 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | June 28, 1984 |
| Decision Date | December 06, 1985 |
| Days to Decision | 526 days |
| Submission Type | Traditional |
| Review Panel | Immunology (IM) |
| Summary | — |
| Product Code | GQO — Antisera, Cf, Herpesvirus Hominis 1,2 |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 866.3305 |