510(k) K223892
K223892 is an FDA 510(k) premarket notification submitted by Innovative Product Brands, Inc. for the device "DentMix VPS Impression Material". The FDA issued a decision of Substantially Equivalent on April 27, 2023. The device falls under product code ELW (Material, Impression), a Class II device regulated under 21 CFR 872.3660. Innovative Product Brands, Inc. has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 27, 2023
- Date Received
- December 28, 2022
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Material, Impression
- Device Class
- Class II
- Regulation Number
- 872.3660
- Review Panel
- DE
- Submission Type