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FDA 510(k)

Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITE

K-Number: K170835 · 2018-06-15

ApplicantHightech Development
Decision Date2018-06-15
Product CodeEGJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITE is a medical device manufactured by Hightech Development. It received FDA 510(k) clearance on 2018-06-15 under approval number K170835. 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 Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITE?

Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITE is a medical device that received FDA 510(k) clearance on 2018-06-15. It is manufactured by Hightech Development. The 510(k) number is K170835.

When was Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITE approved by the FDA?

Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITE received FDA 510(k) clearance on 2018-06-15, under approval number K170835.

What company makes Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITE?

Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITE is manufactured by Hightech Development.

What is the FDA product code for Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITE?

The FDA product code for Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITE is EGJ.

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Official Source

View on FDA Database →

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

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