Periotest
by Siemens Medical Solutions USA, Inc.
510(k) K872171
Periotest is a Class I device made by Siemens Medical Solutions USA, Inc., cleared under FDA 510(k) K872171 on 23 Jun 1987, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK872171 | Date23 Jun 1987 | StatusActive |
Official records
- FDA 510(k) database K872171
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- EKX
- Device class
- Class I
- Regulation
- 21 CFR Part 872.4200
- Advisory committee
- Dental
- FDA decision
- SESE Substantially Equivalent
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