AB BELT PRO— 510(k) K020429
Substantially EquivalentThe Dezac Group
FDA 510(k) clearance K020429 for AB BELT PRO, Substantially Equivalent on 2002-09-13. Applicant: The Dezac Group. Device class: 2.
Clearance details
- Applicant
- The Dezac Group
- Product code
- Code NGX
- Device class
- Class 2
- Regulation
- 21 CFR 890.5850
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington, DC, US
Recent devices under product code NGX
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