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FDA 510(k)

Dermadry

K-Number: K192749 · 2020-02-10

ApplicantDermadry Laboratories, Inc.
Decision Date2020-02-10
Product CodeEGJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Dermadry is a medical device manufactured by Dermadry Laboratories, Inc.. It received FDA 510(k) clearance on 2020-02-10 under approval number K192749. The device is classified under product code EGJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Dermadry?

Dermadry is a medical device that received FDA 510(k) clearance on 2020-02-10. It is manufactured by Dermadry Laboratories, Inc.. The 510(k) number is K192749.

When was Dermadry approved by the FDA?

Dermadry received FDA 510(k) clearance on 2020-02-10, under approval number K192749.

What company makes Dermadry?

Dermadry is manufactured by Dermadry Laboratories, Inc..

What is the FDA product code for Dermadry?

The FDA product code for Dermadry is EGJ.

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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.

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