Dermadry— 510(k) K192749

Substantially Equivalent

Dermadry Laboratories, Inc.

FDA 510(k) clearance K192749 for Dermadry, Substantially Equivalent on 2020-02-10. Applicant: Dermadry Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Dermadry Laboratories, Inc.
Product code: Code EGJ
Device class: Class 2
Regulation: 21 CFR 890.5525
Advisory panel: Physical Medicine
Date received: 2019-09-30
Decision date: 2020-02-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Montreal, CA

Download summary PDF View on FDA.gov ↗

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