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FDA 510(k)

ALLGRAD 45 AND 90 CELL SEPARATION MEDIA

K-Number: K022330 · 2002-08-26

Applicant<Genx> Intl., Inc.
Decision Date2002-08-26
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ALLGRAD 45 AND 90 CELL SEPARATION MEDIA is the device name listed in this FDA 510(k) record. The listed applicant is <Genx> Intl., Inc.. It received FDA 510(k) clearance on 2002-08-26 under 510(k) number K022330. The device is classified under product code MQL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALLGRAD 45 AND 90 CELL SEPARATION MEDIA?

ALLGRAD 45 AND 90 CELL SEPARATION MEDIA is a medical device that received FDA 510(k) clearance on 2002-08-26. The listed applicant is <Genx> Intl., Inc.. The 510(k) number is K022330.

When did ALLGRAD 45 AND 90 CELL SEPARATION MEDIA receive FDA 510(k) clearance?

ALLGRAD 45 AND 90 CELL SEPARATION MEDIA received FDA 510(k) clearance on 2002-08-26, under 510(k) number K022330.

Who is the listed applicant for ALLGRAD 45 AND 90 CELL SEPARATION MEDIA?

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

What is the FDA product code for ALLGRAD 45 AND 90 CELL SEPARATION MEDIA?

The FDA product code for ALLGRAD 45 AND 90 CELL SEPARATION MEDIA is MQL.

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Related Devices (Code: MQL)

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.

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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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