510(k) K170101
K170101 is an FDA 510(k) premarket notification submitted by Inter-Med/Vista Dental Products for the device "Valiant Curing Light". The FDA issued a decision of Substantially Equivalent on June 8, 2017. The device falls under product code EBZ (Activator, Ultraviolet, For Polymerization), a Class II device regulated under 21 CFR 872.6070. Inter-Med/Vista Dental Products has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 8, 2017
- Date Received
- January 11, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Activator, Ultraviolet, For Polymerization
- Device Class
- Class II
- Regulation Number
- 872.6070
- Review Panel
- DE
- Submission Type