The following data is part of a premarket notification filed by Institute Virion Ltd. with the FDA for Varicella/zoster Virus.
| Device ID | K843676 |
| 510k Number | K843676 |
| Device Name: | VARICELLA/ZOSTER VIRUS |
| Classification | Antigen, Cf, (including Cf Control), Varicella-zoster |
| Applicant | INSTITUTE VIRION LTD. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GQW |
| CFR Regulation Number | 866.3900 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-09-17 |
| Decision Date | 1985-09-26 |