The following data is part of a premarket notification filed by Brainlab Ag with the FDA for Table Tilt Device.
| Device ID | K033316 |
| 510k Number | K033316 |
| Device Name: | TABLE TILT DEVICE |
| Classification | Couch, Radiation Therapy, Powered |
| Applicant | BRAINLAB AG AMMERTHALSTRASSE 8 Heimstetten, DE 85551 |
| Contact | Rainer Birkenbach |
| Correspondent | Rainer Birkenbach BRAINLAB AG AMMERTHALSTRASSE 8 Heimstetten, DE 85551 |
| Product Code | JAI |
| CFR Regulation Number | 892.5770 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-10-15 |
| Decision Date | 2004-05-14 |
| Summary: | summary |