The following data is part of a premarket notification filed by Armkel, Llc. with the FDA for Virogen Herpes Slide Test.
| Device ID | K852928 |
| 510k Number | K852928 |
| Device Name: | VIROGEN HERPES SLIDE TEST |
| Classification | Antisera, Cf, Herpesvirus Hominis 1,2 |
| Applicant | ARMKEL, LLC. HALF ACRE RD. P.O. BOX 1001 Cranbury, NJ 08512 |
| Contact | Stephen C Ko0lakows |
| Correspondent | Stephen C Ko0lakows ARMKEL, LLC. HALF ACRE RD. P.O. BOX 1001 Cranbury, NJ 08512 |
| Product Code | GQO |
| CFR Regulation Number | 866.3305 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-07-09 |
| Decision Date | 1985-10-17 |