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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 the device name listed in this FDA 510(k) record. The listed applicant is Q For Plastic Industries. It received FDA 510(k) clearance on 2024-01-03 under 510(k) 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. The listed applicant is Q For Plastic Industries. The 510(k) number is K231707.

When did ResQ Administration Set receive FDA 510(k) clearance?

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

Who is the listed applicant for ResQ Administration Set?

The FDA 510(k) record lists Q For Plastic Industries as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ResQ Administration Set?

The FDA product code for ResQ Administration Set is FPA.

Related Devices (Code: FPA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.