510(k) K151996
K151996 is an FDA 510(k) premarket notification submitted by Shinhung Company, Ltd. for the device "TAURUS C1". The FDA issued a decision of Substantially Equivalent on January 22, 2016. The device falls under product code EIA (Unit, Operative Dental), a Class I device regulated under 21 CFR 872.6640. Shinhung Company, Ltd. has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 22, 2016
- Date Received
- July 20, 2015
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Unit, Operative Dental
- Device Class
- Class I
- Regulation Number
- 872.6640
- Review Panel
- DE
- Submission Type