510(k) K060317
K060317 is an FDA 510(k) premarket notification submitted by Est. Anthogyr for the device "ANTHOGYR CONTRA ANGLES AND HANDPIECES". The FDA issued a decision of Substantially Equivalent on April 28, 2006. The device falls under product code EGS (Handpiece, Contra- And Right-Angle Attachment, Dental), a Class I device regulated under 21 CFR 872.4200. Est. Anthogyr has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 28, 2006
- Date Received
- February 8, 2006
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Handpiece, Contra- And Right-Angle Attachment, Dental
- Device Class
- Class I
- Regulation Number
- 872.4200
- Review Panel
- DE
- Submission Type