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FDA 510(k)

LenSX Laser System

K号: K161288 · 2016-11-16

决定日期2016-11-16
产品代码OOE
咨询委员会OP
决定Substantially Equivalent

器械摘要

LenSX Laser System is the device name listed in this FDA 510(k) record. The listed applicant is Alcon Laboratories, Inc.. It received FDA 510(k) clearance on 2016-11-16 under 510(k) number K161288. The device is classified under product code OOE. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the LenSX Laser System?

LenSX Laser System is a medical device that received FDA 510(k) clearance on 2016-11-16. The listed applicant is Alcon Laboratories, Inc.. The 510(k) number is K161288.

When did LenSX Laser System receive FDA 510(k) clearance?

LenSX Laser System received FDA 510(k) clearance on 2016-11-16, under 510(k) number K161288.

Who is the listed applicant for LenSX Laser System?

The FDA 510(k) record lists Alcon Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LenSX Laser System?

The FDA product code for LenSX Laser System is OOE.

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列明Alcon Laboratories, Inc.为申报人的其他记录

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相关器械(代码:OOE)

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