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FDA 510(k)

VisCalor

K-Number: K201307 · 2020-07-08

ApplicantVoco GmbH
Decision Date2020-07-08
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VisCalor is a medical device manufactured by Voco GmbH. It received FDA 510(k) clearance on 2020-07-08 under approval number K201307. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VisCalor?

VisCalor is a medical device that received FDA 510(k) clearance on 2020-07-08. It is manufactured by Voco GmbH. The 510(k) number is K201307.

When was VisCalor approved by the FDA?

VisCalor received FDA 510(k) clearance on 2020-07-08, under approval number K201307.

What company makes VisCalor?

VisCalor is manufactured by Voco GmbH.

What is the FDA product code for VisCalor?

The FDA product code for VisCalor is EBF.

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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.

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