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FDA 510(k)

Arrow 0.2 Micron Flat Filter, GVS

K-Number: K222341 · 2023-02-13

ApplicantArrow International, LLC
Decision Date2023-02-13
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

Arrow 0.2 Micron Flat Filter, GVS is the device name listed in this FDA 510(k) record. The listed applicant is Arrow International, LLC. It received FDA 510(k) clearance on 2023-02-13 under 510(k) number K222341. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Arrow 0.2 Micron Flat Filter, GVS?

Arrow 0.2 Micron Flat Filter, GVS is a medical device that received FDA 510(k) clearance on 2023-02-13. The listed applicant is Arrow International, LLC. The 510(k) number is K222341.

When did Arrow 0.2 Micron Flat Filter, GVS receive FDA 510(k) clearance?

Arrow 0.2 Micron Flat Filter, GVS received FDA 510(k) clearance on 2023-02-13, under 510(k) number K222341.

Who is the listed applicant for Arrow 0.2 Micron Flat Filter, GVS?

The FDA 510(k) record lists Arrow International, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Arrow 0.2 Micron Flat Filter, GVS?

The FDA product code for Arrow 0.2 Micron Flat Filter, GVS is CAZ.

Other records listing Arrow International, LLC as applicant

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Related Devices (Code: CAZ)

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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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