FDA 510(k)

FILTER DEVICES

K-Number: K761098 · 1977-01-28

Decision Date1977-01-28

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

FILTER DEVICES is the device name listed in this FDA 510(k) record. The listed applicant is Arrow Intl., Inc.. It received FDA 510(k) clearance on 1977-01-28 under 510(k) number K761098. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FILTER DEVICES?

FILTER DEVICES is a medical device that received FDA 510(k) clearance on 1977-01-28. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K761098.

When did FILTER DEVICES receive FDA 510(k) clearance?

FILTER DEVICES received FDA 510(k) clearance on 1977-01-28, under 510(k) number K761098.

Who is the listed applicant for FILTER DEVICES?

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

What is the FDA product code for FILTER DEVICES?

The FDA product code for FILTER DEVICES is FMI.

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Other records listing Arrow Intl., Inc. as applicant

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Related Devices (Code: FMI)

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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.