Decision Date2016-01-19
Product CodeOAP
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Capillus202 is the device name listed in this FDA 510(k) record. The listed applicant is Capillus, LLC. It received FDA 510(k) clearance on 2016-01-19 under 510(k) number K153618. 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 Capillus202?
Capillus202 is a medical device that received FDA 510(k) clearance on 2016-01-19. The listed applicant is Capillus, LLC. The 510(k) number is K153618.
When did Capillus202 receive FDA 510(k) clearance?
Capillus202 received FDA 510(k) clearance on 2016-01-19, under 510(k) number K153618.
Who is the listed applicant for Capillus202?
The FDA 510(k) record lists Capillus, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Capillus202?
The FDA product code for Capillus202 is OAP.
Other records listing Capillus, LLC as applicant
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.
K192012Capillus 112, Capillus 244K163170Capillus 82, Capillus 202, Capillus 272 Pro, 272 Office Pro, Capillus 302, Capillus 312, and Capillus 352K162994Capillus302, Capillus312, Capillus352K160285Capillus272 Pro, Capillus272 OfficePro, Capillus82, Capillus202
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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.