510(k) K000169
K000169 is an FDA 510(k) premarket notification submitted by Dentsply Intl. for the device "NUPRO PROPHYLAXIS PASTE WITH FLUORIDE AND TRICLOSAN". The FDA issued a decision of Substantially Equivalent on March 24, 2000. The device falls under product code EJR (Agent, Polishing, Abrasive, Oral Cavity), a Class I device regulated under 21 CFR 872.6030. Dentsply Intl. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 24, 2000
- Date Received
- January 20, 2000
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Agent, Polishing, Abrasive, Oral Cavity
- Device Class
- Class I
- Regulation Number
- 872.6030
- Review Panel
- DE
- Submission Type