The following data is part of a premarket notification filed by D&r X-ray Products, Inc. with the FDA for Tilting Table Radiographic A9006 Tomojupiter.
Device ID | K850948 |
510k Number | K850948 |
Device Name: | TILTING TABLE RADIOGRAPHIC A9006 TOMOJUPITER |
Classification | Table, Radiographic, Tilting |
Applicant | D&R X-RAY PRODUCTS, INC. 2428 HANOVER AVE. Richmond, VA 23220 |
Contact | David P Armstrong |
Correspondent | David P Armstrong D&R X-RAY PRODUCTS, INC. 2428 HANOVER AVE. Richmond, VA 23220 |
Product Code | IXR |
CFR Regulation Number | 892.1980 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-03-07 |
Decision Date | 1985-04-10 |