510(k) K875340
K875340 is an FDA 510(k) premarket notification submitted by Young Dental Manufacturing Co. 1, LLC for the device "JETPOLISHER(TM)". The FDA issued a decision of Substantially Equivalent on June 10, 1988. The device falls under product code KOJ (Airbrush), a Class II device regulated under 21 CFR 872.6080. 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 10, 1988
- Date Received
- December 30, 1987
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Airbrush
- Device Class
- Class II
- Regulation Number
- 872.6080
- Review Panel
- DE
- Submission Type