510(k) K770997
K770997 is an FDA 510(k) premarket notification submitted by Young Dental Manufacturing Co. 1, LLC for the device "PRO-CARE". The FDA issued a decision of Substantially Equivalent on June 20, 1977. The device falls under product code JEQ (Toothbrush, Powered), a Class I device regulated under 21 CFR 872.6865. Young Dental Manufacturing Co. 1, LLC has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 20, 1977
- Date Received
- June 1, 1977
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Toothbrush, Powered
- Device Class
- Class I
- Regulation Number
- 872.6865
- Review Panel
- DE
- Submission Type