The following data is part of a premarket notification filed by Comet Ltd. C/o Radiology Resources, Inc. with the FDA for Various X-ray Tubes.
Device ID | K911695 |
510k Number | K911695 |
Device Name: | VARIOUS X-RAY TUBES |
Classification | Assembly, Tube Housing, X-ray, Diagnostic |
Applicant | COMET LTD. C/O RADIOLOGY RESOURCES, INC. WALDEGGSTRASSE 72 CH-3097 LIEBEFELD-BERNE Switzerland, CH |
Contact | Veith |
Correspondent | Veith COMET LTD. C/O RADIOLOGY RESOURCES, INC. WALDEGGSTRASSE 72 CH-3097 LIEBEFELD-BERNE Switzerland, CH |
Product Code | ITY |
CFR Regulation Number | 892.1760 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-04-16 |
Decision Date | 1991-06-19 |