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)

illumiflow 148 Laser Cap

K-Number: K173843 · 2018-01-26

ApplicantEglobal, LLC
Decision Date2018-01-26
Product CodeOAP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

illumiflow 148 Laser Cap is a medical device manufactured by Eglobal, LLC. It received FDA 510(k) clearance on 2018-01-26 under approval number K173843. 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 illumiflow 148 Laser Cap?

illumiflow 148 Laser Cap is a medical device that received FDA 510(k) clearance on 2018-01-26. It is manufactured by Eglobal, LLC. The 510(k) number is K173843.

When was illumiflow 148 Laser Cap approved by the FDA?

illumiflow 148 Laser Cap received FDA 510(k) clearance on 2018-01-26, under approval number K173843.

What company makes illumiflow 148 Laser Cap?

illumiflow 148 Laser Cap is manufactured by Eglobal, LLC.

What is the FDA product code for illumiflow 148 Laser Cap?

The FDA product code for illumiflow 148 Laser Cap is OAP.

Other Devices by Eglobal, LLC

K162071IllumiFlow Laser Cap

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.

↑