510(k) K890668
K890668 is an FDA 510(k) premarket notification submitted by Lincoln Park Dental Laboratory for the device "CLEAN DENT". The FDA issued a decision of Substantially Equivalent on April 17, 1989. The device falls under product code EFT (Cleanser, Denture, Over The Counter), a Class I device regulated under 21 CFR 872.3520.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 17, 1989
- Date Received
- February 9, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Cleanser, Denture, Over The Counter
- Device Class
- Class I
- Regulation Number
- 872.3520
- Review Panel
- DE
- Submission Type