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FDA 510(k)

Capillus272 Pro, Capillus272 OfficePro, Capillus82, Capillus202

K-Number: K160285 · 2016-04-25

ApplicantCapillus, LLC
Decision Date2016-04-25
Product CodeOAP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Capillus272 Pro, Capillus272 OfficePro, Capillus82, Capillus202 is a medical device manufactured by Capillus, LLC. It received FDA 510(k) clearance on 2016-04-25 under approval number K160285. 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 Capillus272 Pro, Capillus272 OfficePro, Capillus82, Capillus202?

Capillus272 Pro, Capillus272 OfficePro, Capillus82, Capillus202 is a medical device that received FDA 510(k) clearance on 2016-04-25. It is manufactured by Capillus, LLC. The 510(k) number is K160285.

When was Capillus272 Pro, Capillus272 OfficePro, Capillus82, Capillus202 approved by the FDA?

Capillus272 Pro, Capillus272 OfficePro, Capillus82, Capillus202 received FDA 510(k) clearance on 2016-04-25, under approval number K160285.

What company makes Capillus272 Pro, Capillus272 OfficePro, Capillus82, Capillus202?

Capillus272 Pro, Capillus272 OfficePro, Capillus82, Capillus202 is manufactured by Capillus, LLC.

What is the FDA product code for Capillus272 Pro, Capillus272 OfficePro, Capillus82, Capillus202?

The FDA product code for Capillus272 Pro, Capillus272 OfficePro, Capillus82, Capillus202 is OAP.

Other Devices by Capillus, LLC

K162994Capillus302, Capillus312, Capillus352 K153618Capillus202 K163170Capillus 82, Capillus 202, Capillus 272 Pro, 272 Office Pro, Capillus 302, Capillus 312, and Capillus 352

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. K152587DermaScalp Laser CapDermascalp, LLC K153618Capillus202Capillus, 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.

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