510(k) K890043
K890043 is an FDA 510(k) premarket notification submitted by K-P Co. for the device "DENTCLEAN CONCENTRATED DENTURE CLEANSER". The FDA issued a decision of Substantially Equivalent on June 7, 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
- June 7, 1989
- Date Received
- January 5, 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