The following data is part of a premarket notification filed by Gendex Corp. with the FDA for Visualix Radiographic Image Detecting And Process.
Device ID | K925094 |
510k Number | K925094 |
Device Name: | VISUALIX RADIOGRAPHIC IMAGE DETECTING AND PROCESS |
Classification | Unit, X-ray, Extraoral With Timer |
Applicant | GENDEX CORP. 901 WEST OAKTON ST. Des Plaines, IL 60018 |
Contact | James E Ketner |
Correspondent | James E Ketner GENDEX CORP. 901 WEST OAKTON ST. Des Plaines, IL 60018 |
Product Code | EHD |
CFR Regulation Number | 872.1800 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-10-07 |
Decision Date | 1993-09-29 |