510(k) K033356
K033356 is an FDA 510(k) premarket notification submitted by Aalba Dent, Inc. for the device "VERASOFT ES". The FDA issued a decision of Substantially Equivalent on December 30, 2003. The device falls under product code EJH (Alloy, Metal, Base), a Class II device regulated under 21 CFR 872.3710. Aalba Dent, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 30, 2003
- Date Received
- September 20, 2003
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Alloy, Metal, Base
- Device Class
- Class II
- Regulation Number
- 872.3710
- Review Panel
- DE
- Submission Type