The following data is part of a premarket notification filed by Wuestec Medical, Inc. with the FDA for Xrt 400.
| Device ID | K955414 |
| 510k Number | K955414 |
| Device Name: | XRT 400 |
| Classification | Table, Radiologic |
| Applicant | WUESTEC MEDICAL, INC. 421 HOLCOLMBE AVE. Mobile, AL 36606 |
| Contact | Jim Miller |
| Correspondent | Jim Miller WUESTEC MEDICAL, INC. 421 HOLCOLMBE AVE. Mobile, AL 36606 |
| Product Code | KXJ |
| CFR Regulation Number | 892.1980 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-11-27 |
| Decision Date | 1996-07-24 |