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FDA 510(k)

Squirt Fluid Delivery System

K-Number: K162777 · 2016-10-31

ApplicantMerit Medical Systems, Inc.
Decision Date2016-10-31
Product CodeQEY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

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.

Frequently Asked Questions

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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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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