The following data is part of a premarket notification filed by Gendex Corp. with the FDA for Gendex Prince 30 Medical X-ray Generator.
Device ID | K854499 |
510k Number | K854499 |
Device Name: | GENDEX PRINCE 30 MEDICAL X-RAY GENERATOR |
Classification | Generator, High-voltage, X-ray, Diagnostic |
Applicant | GENDEX CORP. 11341 W. MELROSE ST. Franklin Park, IL 60131 |
Contact | Gerald V Levy |
Correspondent | Gerald V Levy GENDEX CORP. 11341 W. MELROSE ST. Franklin Park, IL 60131 |
Product Code | IZO |
CFR Regulation Number | 892.1700 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-11-12 |
Decision Date | 1986-04-22 |