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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 the device name listed in this FDA 510(k) record. The listed applicant is Voco GmbH. It received FDA 510(k) clearance on 2020-07-08 under 510(k) 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. The listed applicant is Voco GmbH. The 510(k) number is K201307.

When did VisCalor receive FDA 510(k) clearance?

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

Who is the listed applicant for VisCalor?

The FDA 510(k) record lists Voco GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VisCalor?

The FDA product code for VisCalor is EBF.

Other records listing Voco GmbH as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 29 devices →

Related Devices (Code: EBF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.