SIREMAT
System, X-ray, Stationary
SIEMENS CORP.
The following data is part of a premarket notification filed by Siemens Corp. with the FDA for Siremat.
Pre-market Notification Details
| Device ID | K781613 |
| 510k Number | K781613 |
| Device Name: | SIREMAT |
| 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 | 1978-09-19 |
| Decision Date | 1978-10-03 |
Trademark Results [SIREMAT]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SIREMAT 73119148 1079779 Dead/Expired |
SIEMENS AKTIENGESELLSCHAFT 1977-03-15 |
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