510(k) K220873
K220873 is an FDA 510(k) premarket notification submitted by Lares Research for the device "Perceptive electric dental motor and control unit". The FDA issued a decision of Substantially Equivalent on December 15, 2022. The device falls under product code EIA (Unit, Operative Dental), a Class I device regulated under 21 CFR 872.6640. Lares Research has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 15, 2022
- Date Received
- March 25, 2022
- 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