VistaCam iX Proof
K-Number: K150672 · 2016-01-27
ApplicantDurr Dental AG
Decision Date2016-01-27
Product CodeNBL
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
VistaCam iX Proof is a medical device manufactured by Durr Dental AG. It received FDA 510(k) clearance on 2016-01-27 under approval number K150672. The device is classified under product code NBL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the VistaCam iX Proof?
VistaCam iX Proof is a medical device that received FDA 510(k) clearance on 2016-01-27. It is manufactured by Durr Dental AG. The 510(k) number is K150672.
When was VistaCam iX Proof approved by the FDA?
VistaCam iX Proof received FDA 510(k) clearance on 2016-01-27, under approval number K150672.
What company makes VistaCam iX Proof?
VistaCam iX Proof is manufactured by Durr Dental AG.
What is the FDA product code for VistaCam iX Proof?
The FDA product code for VistaCam iX Proof is NBL.
Other Devices by Durr Dental AG
Related Devices (Code: NBL)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.