Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

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 a medical device manufactured by Advihair S.R.L.. It received FDA 510(k) clearance on 2020-12-03 under approval 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. It is manufactured by Advihair S.R.L.. The 510(k) number is K193008.

When was Tricoglam Home Use approved by the FDA?

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

What company makes Tricoglam Home Use?

Tricoglam Home Use is manufactured by Advihair S.R.L..

What is the FDA product code for Tricoglam Home Use?

The FDA product code for Tricoglam Home Use is OAP.

Related Devices (Code: OAP)

K162994Capillus302, Capillus312, Capillus352Capillus, LLC K161875LaserCap300, LaserCap224, LaserCap120, LaserCap80Transdermal Cap, Inc. K160728NutraStim Hair Laser HelmetNutra Luxe MD, LLC K161046Laser Helmet LH40-EVOTheradome, Inc. K160285Capillus272 Pro, Capillus272 OfficePro, Capillus82, Capillus202Capillus, LLC K152587DermaScalp Laser CapDermascalp, LLC

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.

↑