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Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITE

K170835 Class II Traditional
Decision Date
2018-06-15
Sponsor / Applicant
Hightech Development

Technical Specification

510(k) Submission ID K170835
Product Code EGJ
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5525
Decision Date 2018-06-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITE received FDA 510(k) clearance under submission number K170835, sponsored by Hightech Development. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2018-06-15.

Classification & Regulation

This clearance is catalogued under FDA product code EGJ and 21 CFR 890.5525, within the Physical Medicine review panel as a Class II device.