510(k) K951607
K951607 is an FDA 510(k) premarket notification submitted by Dentsply Intl. for the device "SUREFLEX FILES". The FDA issued a decision of Substantially Equivalent on June 22, 1995. The device falls under product code EKJ (Burnisher, Operative), a Class I device regulated under 21 CFR 872.4565. Dentsply Intl. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 22, 1995
- Date Received
- March 16, 1995
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Burnisher, Operative
- Device Class
- Class I
- Regulation Number
- 872.4565
- Review Panel
- DE
- Submission Type