FDA 510(k)

ResQ Administration Set

K-Number: K231707 · 2024-01-03

Decision Date2024-01-03

Product CodeFPA

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

ResQ Administration Set is a medical device manufactured by Q For Plastic Industries. It received FDA 510(k) clearance on 2024-01-03 under approval number K231707. 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 ResQ Administration Set?

ResQ Administration Set is a medical device that received FDA 510(k) clearance on 2024-01-03. It is manufactured by Q For Plastic Industries. The 510(k) number is K231707.

When was ResQ Administration Set approved by the FDA?

ResQ Administration Set received FDA 510(k) clearance on 2024-01-03, under approval number K231707.

What company makes ResQ Administration Set?

ResQ Administration Set is manufactured by Q For Plastic Industries.

What is the FDA product code for ResQ Administration Set?

The FDA product code for ResQ Administration Set is FPA.

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Official Source

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