Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITE— 510(k) K170835

Name: FDA 510(k) clearance K170835
Creator: U.S. Food and Drug Administration
Published: 2018-06-15

Substantially Equivalent

Hightech Development

FDA 510(k) clearance K170835 for Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITE, Substantially Equivalent on 2018-06-15. Applicant: Hightech Development. Device class: 2.

Clearance details

Applicant: Hightech Development
Product code: Code EGJ
Device class: Class 2
Regulation: 21 CFR 890.5525
Advisory panel: Physical Medicine
Date received: 2017-03-20
Decision date: 2018-06-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Prague, CZ

Download summary PDF View on FDA.gov ↗

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