510(k) K951607

SUREFLEX FILES by Dentsply Intl. — Product Code EKJ

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