510(k) K000799
K000799 is an FDA 510(k) premarket notification submitted by Belmont Equipment Corp. for the device "BELMONT UNIT, MODEL 2000 SERIES". The FDA issued a decision of Substantially Equivalent on May 17, 2000. The device falls under product code EIA (Unit, Operative Dental), a Class I device regulated under 21 CFR 872.6640. Belmont Equipment Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 17, 2000
- Date Received
- March 13, 2000
- 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