510(k) K871636
K871636 is an FDA 510(k) premarket notification submitted by Kuraray Co. for the device "CLEARFIL PORCELAIN BOND". The FDA issued a decision of Substantially Equivalent on July 2, 1987. The device falls under product code KLE (Agent, Tooth Bonding, Resin), a Class II device regulated under 21 CFR 872.3200. Kuraray Co. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 2, 1987
- Date Received
- April 27, 1987
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Agent, Tooth Bonding, Resin
- Device Class
- Class II
- Regulation Number
- 872.3200
- Review Panel
- DE
- Submission Type