510(k) K791716
K791716 is an FDA 510(k) premarket notification submitted by Noxell for the device "PLAQUE-X DENTURE CLEANSER". The FDA issued a decision of Substantially Equivalent on October 23, 1979. The device falls under product code JER (Cleaner, Denture, Mechanical), a Class I device regulated under 21 CFR 872.3530.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 23, 1979
- Date Received
- August 31, 1979
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Cleaner, Denture, Mechanical
- Device Class
- Class I
- Regulation Number
- 872.3530
- Review Panel
- DE
- Submission Type