The following data is part of a premarket notification filed by D&r X-ray Products, Inc. with the FDA for Radiographic Tables Models A71os-t,a71ot-t,a71ob-t.
Device ID | K861940 |
510k Number | K861940 |
Device Name: | RADIOGRAPHIC TABLES MODELS A71OS-T,A71OT-T,A71OB-T |
Classification | Table, Radiographic, Non-tilting, Powered |
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 | IZZ |
CFR Regulation Number | 892.1980 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-05-20 |
Decision Date | 1986-05-29 |