The following data is part of a premarket notification filed by Prowess, Inc. with the FDA for Prowess Panther Proarc, Model Version 5.0.
| Device ID | K101076 |
| 510k Number | K101076 |
| Device Name: | PROWESS PANTHER PROARC, MODEL VERSION 5.0 |
| Classification | System, Planning, Radiation Therapy Treatment |
| Applicant | PROWESS, INC. 1844 CLAYTON ROAD Concord, CA 94520 |
| Contact | Rachel Scarano |
| Correspondent | Rachel Scarano PROWESS, INC. 1844 CLAYTON ROAD Concord, CA 94520 |
| Product Code | MUJ |
| CFR Regulation Number | 892.5050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-04-19 |
| Decision Date | 2010-07-27 |
| Summary: | summary |