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FDA 510(k)

Q2 Low Pressure Power Injection Extension Set

K-Number: K162804 · 2017-03-08

ApplicantQuest Medical, Inc.
Decision Date2017-03-08
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Q2 Low Pressure Power Injection Extension Set is a medical device manufactured by Quest Medical, Inc.. It received FDA 510(k) clearance on 2017-03-08 under approval number K162804. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Q2 Low Pressure Power Injection Extension Set?

Q2 Low Pressure Power Injection Extension Set is a medical device that received FDA 510(k) clearance on 2017-03-08. It is manufactured by Quest Medical, Inc.. The 510(k) number is K162804.

When was Q2 Low Pressure Power Injection Extension Set approved by the FDA?

Q2 Low Pressure Power Injection Extension Set received FDA 510(k) clearance on 2017-03-08, under approval number K162804.

What company makes Q2 Low Pressure Power Injection Extension Set?

Q2 Low Pressure Power Injection Extension Set is manufactured by Quest Medical, Inc..

What is the FDA product code for Q2 Low Pressure Power Injection Extension Set?

The FDA product code for Q2 Low Pressure Power Injection Extension Set is FPA.

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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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