The following data is part of a premarket notification filed by Ion Beam Applications S.a. with the FDA for Gantry Beam Line.
| Device ID | K132919 |
| 510k Number | K132919 |
| Device Name: | GANTRY BEAM LINE |
| Classification | System, Radiation Therapy, Charged-particle, Medical |
| Applicant | ION BEAM APPLICATIONS S.A. 1500 MARKET STREET CENTRE SQUARE WEST, 38TH FLOOR Philadelphia, PA 19102 |
| Contact | Bruce D Armon |
| Correspondent | Bruce D Armon ION BEAM APPLICATIONS S.A. 1500 MARKET STREET CENTRE SQUARE WEST, 38TH FLOOR Philadelphia, PA 19102 |
| Product Code | LHN |
| CFR Regulation Number | 892.5050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-09-17 |
| Decision Date | 2014-07-10 |
| Summary: | summary |