510(k) K955521
K955521 is an FDA 510(k) premarket notification submitted by Wallace A. Erickson & Co. for the device "ALPHA-DENT COPAL CAVITY VARNISH". The FDA issued a decision of Substantially Equivalent on January 24, 1996. The device falls under product code LBH (Varnish, Cavity), a Class II device regulated under 21 CFR 872.3260. Wallace A. Erickson & Co. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 24, 1996
- Date Received
- December 4, 1995
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Varnish, Cavity
- Device Class
- Class II
- Regulation Number
- 872.3260
- Review Panel
- DE
- Submission Type