DANTEC COUNTERPOINT MK2(TM)— 510(k) K913957
Substantially EquivalentDantec Medical, Inc.
FDA 510(k) clearance K913957 for DANTEC COUNTERPOINT MK2(TM), Substantially Equivalent on 1992-01-30. Applicant: Dantec Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Dantec Medical, Inc.
- Product code
- Code GWJ
- Device class
- Class 2
- Regulation
- 21 CFR 882.1900
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington, DC, US
Recent devices under product code GWJ
view allMore clearances from Dantec Medical, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.