510(k) K772314
K772314 is an FDA 510(k) premarket notification submitted by Den-Mat Corp. for the device "WEDGES, RETAINING, MATRIX". The FDA issued a decision of Substantially Equivalent on January 3, 1978. The device falls under product code DZN (Instruments, Dental Hand), a Class I device regulated under 21 CFR 872.4565. Den-Mat Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 3, 1978
- Date Received
- December 19, 1977
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Instruments, Dental Hand
- Device Class
- Class I
- Regulation Number
- 872.4565
- Review Panel
- DE
- Submission Type