510(k) K801142
K801142 is an FDA 510(k) premarket notification submitted by Alvin Meyer, D.D.S. for the device "PALODENT MATRICES & BITINE RINGS". The FDA issued a decision of Substantially Equivalent on August 7, 1980. The device falls under product code DZN (Instruments, Dental Hand), a Class I device regulated under 21 CFR 872.4565.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 7, 1980
- Date Received
- May 13, 1980
- 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