FDA 510(k)

ポケット型コルポスコープシステム

K番号: K181034 · 2018-09-21

決定日2018-09-21

製品コードHEX

諮問委員会医薬品機器規制テキストの翻訳は以下の通りです。 [原文] OB [翻訳] OB

決定Substantially Equivalent

医療機器の概要

Pocket Colposcope System is the device name listed in this FDA 510(k) record. The listed applicant is Hadleigh Health Technologies, LLC. It received FDA 510(k) clearance on 2018-09-21 under 510(k) number K181034. The device is classified under product code HEX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the Pocket Colposcope System?

Pocket Colposcope System is a medical device that received FDA 510(k) clearance on 2018-09-21. The listed applicant is Hadleigh Health Technologies, LLC. The 510(k) number is K181034.

When did Pocket Colposcope System receive FDA 510(k) clearance?

Pocket Colposcope System received FDA 510(k) clearance on 2018-09-21, under 510(k) number K181034.

Who is the listed applicant for Pocket Colposcope System?

The FDA 510(k) record lists Hadleigh Health Technologies, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Pocket Colposcope System?

The FDA product code for Pocket Colposcope System is HEX.

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ポケット型コルポスコープシステム

医療機器の概要

よくある質問

関連する臨床試験

関連機器（コード：HEX）

公式ソース