510(k) K151852
K151852 is an FDA 510(k) premarket notification submitted by Pac-Dent International, Inc. for the device "PacEndo Sodium Hyprochlorite". The FDA issued a decision of Substantially Equivalent on November 10, 2015. The device falls under product code KJJ (Cleanser, Root Canal), a Class U device. Pac-Dent International, Inc. has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 10, 2015
- Date Received
- July 7, 2015
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Cleanser, Root Canal
- Device Class
- Class U
- Regulation Number
- Review Panel
- DE
- Submission Type