The following data is part of a premarket notification filed by Wuestec Medical, Inc. with the FDA for Movable Cantilevered Radiographic Table Xrt 100, 200 & 300.
Device ID | K960083 |
510k Number | K960083 |
Device Name: | MOVABLE CANTILEVERED RADIOGRAPHIC TABLE XRT 100, 200 & 300 |
Classification | Table, Radiographic, Stationary Top |
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 | IXQ |
CFR Regulation Number | 892.1980 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-01-11 |
Decision Date | 1996-07-24 |