Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITE
K-Number: K170835 · 2018-06-15
Device Summary
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. The listed applicant is Hightech Development. The 510(k) number is K170835.
When did Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITE receive FDA 510(k) clearance?
Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITE received FDA 510(k) clearance on 2018-06-15, under 510(k) number K170835.
Who is the listed applicant for Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITE?
The FDA 510(k) record lists Hightech Development as the applicant. This does not by itself establish the device manufacturer.
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.
Related Devices (Code: EGJ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.