VOCO Retraction Paste
K-Number: K213149 · 2021-12-09
Device Summary
VOCO Retraction Paste is a medical device manufactured by Voco GmbH. It received FDA 510(k) clearance on 2021-12-09 under approval number K213149. The device is classified under product code MVL. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the VOCO Retraction Paste?
VOCO Retraction Paste is a medical device that received FDA 510(k) clearance on 2021-12-09. It is manufactured by Voco GmbH. The 510(k) number is K213149.
When was VOCO Retraction Paste approved by the FDA?
VOCO Retraction Paste received FDA 510(k) clearance on 2021-12-09, under approval number K213149.
What company makes VOCO Retraction Paste?
VOCO Retraction Paste is manufactured by Voco GmbH.
What is the FDA product code for VOCO Retraction Paste?
The FDA product code for VOCO Retraction Paste is MVL.
Other Devices by Voco GmbH
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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.