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FDA 510(k)

QUADRASORB FILTER

K-Number: K923661 · 1992-10-20

ApplicantUnion Broach, Div. Moyco Industries, Inc.
Decision Date1992-10-20
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

QUADRASORB FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Union Broach, Div. Moyco Industries, Inc.. It received FDA 510(k) clearance on 1992-10-20 under 510(k) number K923661. The device is classified under product code CAH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUADRASORB FILTER?

QUADRASORB FILTER is a medical device that received FDA 510(k) clearance on 1992-10-20. The listed applicant is Union Broach, Div. Moyco Industries, Inc.. The 510(k) number is K923661.

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

QUADRASORB FILTER received FDA 510(k) clearance on 1992-10-20, under 510(k) number K923661.

Who is the listed applicant for QUADRASORB FILTER?

The FDA 510(k) record lists Union Broach, Div. Moyco Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QUADRASORB FILTER?

The FDA product code for QUADRASORB FILTER is CAH.

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Other records listing Union Broach, Div. Moyco Industries, Inc. as applicant

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Related Devices (Code: CAH)

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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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