510(k) K891140
K891140 is an FDA 510(k) premarket notification submitted by Coe Laboratories, Inc. for the device "OCCLU-SEAL(TM) VISIBLE LIGHT-CURED FISSURE SEALANT". The FDA issued a decision of Substantially Equivalent on May 1, 1989. The device falls under product code EBC (Sealant, Pit And Fissure, And Conditioner), a Class II device regulated under 21 CFR 872.3765. Coe Laboratories, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 1, 1989
- Date Received
- March 3, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Sealant, Pit And Fissure, And Conditioner
- Device Class
- Class II
- Regulation Number
- 872.3765
- Review Panel
- DE
- Submission Type