The following data is part of a premarket notification filed by Siemens Corp. with the FDA for Trioskop.
Device ID | K792645 |
510k Number | K792645 |
Device Name: | TRIOSKOP |
Classification | Table, Radiographic, Tilting |
Applicant | SIEMENS CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | IXR |
CFR Regulation Number | 892.1980 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1979-12-26 |
Decision Date | 1980-01-28 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TRIOSKOP 73261635 1173043 Dead/Cancelled |
Siemens Aktiengesellschaft 1980-05-12 |