510(k) K082985
K082985 is an FDA 510(k) premarket notification submitted by A-Dec, Inc. for the device "A-DEC 334/335 DELIVERY SYSTEM". The FDA issued a decision of Substantially Equivalent on December 17, 2008. The device falls under product code EIA (Unit, Operative Dental), a Class I device regulated under 21 CFR 872.6640. A-Dec, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 17, 2008
- Date Received
- October 7, 2008
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Unit, Operative Dental
- Device Class
- Class I
- Regulation Number
- 872.6640
- Review Panel
- DE
- Submission Type