The following data is part of a premarket notification filed by Adac Laboratories with the FDA for Pinnacle 3.
| Device ID | K926008 |
| 510k Number | K926008 |
| Device Name: | PINNACLE 3 |
| Classification | Accelerator, Linear, Medical |
| 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 | IYE |
| CFR Regulation Number | 892.5050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-11-27 |
| Decision Date | 1994-10-04 |