PERIOTEST
Handpiece, Direct Drive, Ac-powered
SIEMENS MEDICAL SOLUTIONS USA, INC.
The following data is part of a premarket notification filed by Siemens Medical Solutions Usa, Inc. with the FDA for Periotest.
Pre-market Notification Details
| Device ID | K872171 |
| 510k Number | K872171 |
| Device Name: | PERIOTEST |
| Classification | Handpiece, Direct Drive, Ac-powered |
| Applicant | SIEMENS MEDICAL SOLUTIONS USA, INC. 186 WOOD AVENUE SOUTH Iselin, NJ 08830 |
| Contact | Harry K Schwill |
| Correspondent | Harry K Schwill SIEMENS MEDICAL SOLUTIONS USA, INC. 186 WOOD AVENUE SOUTH Iselin, NJ 08830 |
| Product Code | EKX |
| CFR Regulation Number | 872.4200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-06-08 |
| Decision Date | 1987-06-23 |
Trademark Results [PERIOTEST]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 PERIOTEST 73686882 1494989 Dead/Cancelled |
SIEMENS AKTIENGESELLSCHAFT 1987-09-28 |
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