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FDA 510(k)

Squirt Fluid Delivery System

K 號：K162777 · 2016-10-31

申請人Merit Medical Systems, Inc.
決定日期2016-10-31
產品代碼QEY
諮詢委員會CV
決定Substantially Equivalent

器材摘要

Squirt Fluid Delivery System is the device name listed in this FDA 510(k) record. The listed applicant is Merit Medical Systems, Inc.. It received FDA 510(k) clearance on 2016-10-31 under 510(k) number K162777. The device is classified under product code QEY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Squirt Fluid Delivery System?

Squirt Fluid Delivery System is a medical device that received FDA 510(k) clearance on 2016-10-31. The listed applicant is Merit Medical Systems, Inc.. The 510(k) number is K162777.

When did Squirt Fluid Delivery System receive FDA 510(k) clearance?

Squirt Fluid Delivery System received FDA 510(k) clearance on 2016-10-31, under 510(k) number K162777.

Who is the listed applicant for Squirt Fluid Delivery System?

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

What is the FDA product code for Squirt Fluid Delivery System?

The FDA product code for Squirt Fluid Delivery System is QEY.

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