FDA 510(k)

Capillus 82, Capillus 202, Capillus 272 Pro, 272 Office Pro, Capillus 302, Capillus 312, and Capillus 352

K-번호: K163170 · 2017-01-31

결정일2017-01-31

제품 코드OAP

자문 위원회PM

결정Substantially Equivalent

기기 요약

Capillus 82, Capillus 202, Capillus 272 Pro, 272 Office Pro, Capillus 302, Capillus 312, and Capillus 352 is the device name listed in this FDA 510(k) record. The listed applicant is Capillus, LLC. It received FDA 510(k) clearance on 2017-01-31 under 510(k) number K163170. The device is classified under product code OAP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Capillus 82, Capillus 202, Capillus 272 Pro, 272 Office Pro, Capillus 302, Capillus 312, and Capillus 352?

Capillus 82, Capillus 202, Capillus 272 Pro, 272 Office Pro, Capillus 302, Capillus 312, and Capillus 352 is a medical device that received FDA 510(k) clearance on 2017-01-31. The listed applicant is Capillus, LLC. The 510(k) number is K163170.

When did Capillus 82, Capillus 202, Capillus 272 Pro, 272 Office Pro, Capillus 302, Capillus 312, and Capillus 352 receive FDA 510(k) clearance?

Capillus 82, Capillus 202, Capillus 272 Pro, 272 Office Pro, Capillus 302, Capillus 312, and Capillus 352 received FDA 510(k) clearance on 2017-01-31, under 510(k) number K163170.

Who is the listed applicant for Capillus 82, Capillus 202, Capillus 272 Pro, 272 Office Pro, Capillus 302, Capillus 312, and Capillus 352?

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 Capillus 82, Capillus 202, Capillus 272 Pro, 272 Office Pro, Capillus 302, Capillus 312, and Capillus 352?

The FDA product code for Capillus 82, Capillus 202, Capillus 272 Pro, 272 Office Pro, Capillus 302, Capillus 312, and Capillus 352 is OAP.

Capillus, LLC를 신청인으로 등재한 기타 기록

K162994Capillus302, Capillus312, Capillus352 K160285Capillus272 Pro, Capillus272 OfficePro, Capillus82, Capillus202 K153618Capillus202

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