510(k) K182068
K182068 is an FDA 510(k) premarket notification submitted by Hangzhou Erran Technology Co., Ltd. for the device "Erran Dental Zirconia". The FDA issued a decision of Substantially Equivalent on Dec 13, 2018. The device falls under product code EIH (Powder, Porcelain), a Class II device regulated under 21 CFR 872.6660.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Dec 13, 2018
- Date Received
- Aug 1, 2018
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Powder, Porcelain
- Device Class
- Class II
- Regulation Number
- 872.6660
- Review Panel
- DE
- Submission Type
- 510(k)