510(k) K895269
K895269 is an FDA 510(k) premarket notification submitted by Den-Mat Corp. for the device "DEN-MAT LAMI-QUICK". The FDA issued a decision of Substantially Equivalent on February 22, 1990. The device falls under product code ELL (Teeth, Porcelain), a Class II device regulated under 21 CFR 872.3920. Den-Mat Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 22, 1990
- Date Received
- August 23, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Teeth, Porcelain
- Device Class
- Class II
- Regulation Number
- 872.3920
- Review Panel
- DE
- Submission Type