510(k) K193434
K193434 is an FDA 510(k) premarket notification submitted by Vita Zahnfabrik GmbH H Rauter & CO for the device "VITA LUMEX AC". The FDA issued a decision of Substantially Equivalent on July 21, 2020. The device falls under product code EIH (Powder, Porcelain), a Class II device regulated under 21 CFR 872.6660. Vita Zahnfabrik GmbH H Rauter & CO has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 21, 2020
- Date Received
- December 11, 2019
- 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