INTRA SKAN DC— 510(k) K103579
Substantially EquivalentSkanray Technologies
FDA 510(k) clearance K103579 for INTRA SKAN DC, Substantially Equivalent on 2011-03-18. Applicant: Skanray Technologies. Device class: 2.
Clearance details
- Applicant
- Skanray Technologies
- Product code
- Code EHD
- Device class
- Class 2
- Regulation
- 21 CFR 872.1800
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mysore, IN
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