POLYPHOS
Generator, High-voltage, X-ray, Diagnostic
SIEMENS CORP.
The following data is part of a premarket notification filed by Siemens Corp. with the FDA for Polyphos.
Pre-market Notification Details
| Device ID | K792392 |
| 510k Number | K792392 |
| Device Name: | POLYPHOS |
| Classification | Generator, High-voltage, X-ray, Diagnostic |
| Applicant | SIEMENS CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | IZO |
| CFR Regulation Number | 892.1700 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-11-26 |
| Decision Date | 1979-12-20 |
Trademark Results [POLYPHOS]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 POLYPHOS 78819500 3399851 Live/Registered |
Custom Synthesis, LLC 2006-02-21 |
 POLYPHOS 73292884 1185623 Dead/Cancelled |
Siemens Aktiengesellschaft 1981-01-13 |
 POLYPHOS 72115074 0731013 Dead/Cancelled |
Olin Mathieson Chemical Corporation 1961-03-07 |
 POLYPHOS 72114869 0731282 Dead/Cancelled |
Olin Mathieson Chemical Corporation 1961-03-03 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.