The following data is part of a premarket notification filed by Institute Virion Ltd. with the FDA for Chlamydia.
| Device ID | K843654 |
| 510k Number | K843654 |
| Device Name: | CHLAMYDIA |
| Classification | Antigen, Cf, Psittacosis (chlamydia Group) |
| Applicant | INSTITUTE VIRION LTD. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GPW |
| CFR Regulation Number | 866.3120 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-09-17 |
| Decision Date | 1985-08-08 |