510(k) K873123
K873123 is an FDA 510(k) premarket notification submitted by Lee Pharmaceuticals for the device "LEE COMPOSITE INLAY SYSTEM". The FDA issued a decision of Substantially Equivalent on January 20, 1988. The device falls under product code EBF (Material, Tooth Shade, Resin), a Class II device regulated under 21 CFR 872.3690. Lee Pharmaceuticals has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 20, 1988
- Date Received
- August 10, 1987
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Material, Tooth Shade, Resin
- Device Class
- Class II
- Regulation Number
- 872.3690
- Review Panel
- DE
- Submission Type