The following data is part of a premarket notification filed by Nomos Corp. with the FDA for Peacock Plan.
| Device ID | K940663 |
| 510k Number | K940663 |
| Device Name: | PEACOCK PLAN |
| Classification | Accelerator, Linear, Medical |
| Applicant | NOMOS CORP. 2593 WEXFORD BAYNE RD. SUITE 315 Sewickley, PA 15143 |
| Contact | Harris S Targovnik, Ph.d. |
| Correspondent | Harris S Targovnik, Ph.d. NOMOS CORP. 2593 WEXFORD BAYNE RD. SUITE 315 Sewickley, PA 15143 |
| Product Code | IYE |
| CFR Regulation Number | 892.5050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-02-18 |
| Decision Date | 1996-04-09 |
| Summary: | summary |