The following data is part of a premarket notification filed by Adac Laboratories with the FDA for Genesys Ii.
| Device ID | K922080 |
| 510k Number | K922080 |
| Device Name: | GENESYS II |
| Classification | System, Tomography, Computed, Emission |
| Applicant | ADAC LABORATORIES 540 ALDER DR. Milpitas, CA 95035 |
| Contact | Paul Vicha |
| Correspondent | Paul Vicha ADAC LABORATORIES 540 ALDER DR. Milpitas, CA 95035 |
| Product Code | KPS |
| CFR Regulation Number | 892.1200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-05-04 |
| Decision Date | 1992-07-17 |