FDA 510(k)

Capillus272 Pro、Capillus272 OfficePro、Capillus82、Capillus202

K 號：K160285 · 2016-04-25

決定日期2016-04-25

產品代碼OAP

諮詢委員會PM

決定相當於

器材摘要

Capillus272 Pro, Capillus272 OfficePro, Capillus82, 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 2016-04-25 under 510(k) number K160285. The device is classified under product code OAP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

常見問題

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.

其他以 Capillus, LLC 為申請人之記錄

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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

相關器械（代碼：OAP）

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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