The following data is part of a premarket notification filed by Swissray Finatech, Inc. with the FDA for Gen-x 800/800.
Device ID | K914301 |
510k Number | K914301 |
Device Name: | GEN-X 800/800 |
Classification | Generator, High-voltage, X-ray, Diagnostic |
Applicant | SWISSRAY FINATECH, INC. 5621 KALISA CT. Mobile, AL 36693 |
Contact | Michael W Scott |
Correspondent | Michael W Scott SWISSRAY FINATECH, INC. 5621 KALISA CT. Mobile, AL 36693 |
Product Code | IZO |
CFR Regulation Number | 892.1700 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-09-25 |
Decision Date | 1991-10-30 |