Capillus272 Pro, Capillus272 OfficePro, Capillus82, Capillus202
K-Number: K160285 · 2016-04-25
Device Summary
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. The listed applicant is Capillus, LLC. The 510(k) number is K160285.
When did Capillus272 Pro, Capillus272 OfficePro, Capillus82, Capillus202 receive FDA 510(k) clearance?
Capillus272 Pro, Capillus272 OfficePro, Capillus82, Capillus202 received FDA 510(k) clearance on 2016-04-25, under 510(k) number K160285.
Who is the listed applicant for Capillus272 Pro, Capillus272 OfficePro, Capillus82, 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 Capillus272 Pro, Capillus272 OfficePro, Capillus82, Capillus202?
The FDA product code for Capillus272 Pro, Capillus272 OfficePro, Capillus82, 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.
Related Devices (Code: OAP)
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.
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.