The following data is part of a premarket notification filed by Siemens Corp. with the FDA for Buckymat.
Device ID | K790069 |
510k Number | K790069 |
Device Name: | BUCKYMAT |
Classification | System, X-ray, Stationary |
Applicant | SIEMENS CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | KPR |
CFR Regulation Number | 892.1680 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1979-01-12 |
Decision Date | 1979-01-26 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BUCKYMAT 73160432 1124441 Dead/Cancelled |
SIEMENS AKTIENGESELLSCHAFT 1978-03-01 |