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FDA 510(k)

Tricoglam Home Use

K-Number: K193008 · 2020-12-03

ApplicantAdvihair S.R.L.
Decision Date2020-12-03
Product CodeOAP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Tricoglam Home Use is the device name listed in this FDA 510(k) record. The listed applicant is Advihair S.R.L.. It received FDA 510(k) clearance on 2020-12-03 under 510(k) number K193008. The device is classified under product code OAP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Tricoglam Home Use?

Tricoglam Home Use is a medical device that received FDA 510(k) clearance on 2020-12-03. The listed applicant is Advihair S.R.L.. The 510(k) number is K193008.

When did Tricoglam Home Use receive FDA 510(k) clearance?

Tricoglam Home Use received FDA 510(k) clearance on 2020-12-03, under 510(k) number K193008.

Who is the listed applicant for Tricoglam Home Use?

The FDA 510(k) record lists Advihair S.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Tricoglam Home Use?

The FDA product code for Tricoglam Home Use is OAP.

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Official Source

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

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