FDA 510(k)

眼科軟體平台 RX

K 號：K173689 · 2018-02-23

決定日期2018-02-23

產品代碼NFJ

諮詢委員會RA

決定相當於

器材摘要

Ophthalmic Software Platform RX is the device name listed in this FDA 510(k) record. The listed applicant is Canon Inc. -Medical Equipment Group. It received FDA 510(k) clearance on 2018-02-23 under 510(k) number K173689. The device is classified under product code NFJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Ophthalmic Software Platform RX?

Ophthalmic Software Platform RX is a medical device that received FDA 510(k) clearance on 2018-02-23. The listed applicant is Canon Inc. -Medical Equipment Group. The 510(k) number is K173689.

When did Ophthalmic Software Platform RX receive FDA 510(k) clearance?

Ophthalmic Software Platform RX received FDA 510(k) clearance on 2018-02-23, under 510(k) number K173689.

Who is the listed applicant for Ophthalmic Software Platform RX?

The FDA 510(k) record lists Canon Inc. -Medical Equipment Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Ophthalmic Software Platform RX?

The FDA product code for Ophthalmic Software Platform RX is NFJ.

其他以 Canon Inc. -Medical Equipment Group 為申請人之記錄

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相關器械（代碼：NFJ）

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