PERIOTEST— 510(k) K872171
Substantially EquivalentSiemens Medical Solutions USA, Inc.
FDA 510(k) clearance K872171 for PERIOTEST, Substantially Equivalent on 1987-06-23. Applicant: Siemens Medical Solutions USA, Inc.. Device class: 1.
Clearance details
- Applicant
- Siemens Medical Solutions USA, Inc.
- Product code
- Code EKX
- Device class
- Class 1
- Regulation
- 21 CFR 872.4200
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Iselin, NJ, US
Recent devices under product code EKX
view allMore clearances from Siemens Medical Solutions USA, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.