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FDA 510(k)

NEOCARE 20 MICRON BLOOD FILTER

K-Number: K000719 · 2000-05-30

ApplicantWhatman, Inc.
Decision Date2000-05-30
Product CodeCAK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NEOCARE 20 MICRON BLOOD FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Whatman, Inc.. It received FDA 510(k) clearance on 2000-05-30 under 510(k) number K000719. The device is classified under product code CAK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEOCARE 20 MICRON BLOOD FILTER?

NEOCARE 20 MICRON BLOOD FILTER is a medical device that received FDA 510(k) clearance on 2000-05-30. The listed applicant is Whatman, Inc.. The 510(k) number is K000719.

When did NEOCARE 20 MICRON BLOOD FILTER receive FDA 510(k) clearance?

NEOCARE 20 MICRON BLOOD FILTER received FDA 510(k) clearance on 2000-05-30, under 510(k) number K000719.

Who is the listed applicant for NEOCARE 20 MICRON BLOOD FILTER?

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

What is the FDA product code for NEOCARE 20 MICRON BLOOD FILTER?

The FDA product code for NEOCARE 20 MICRON BLOOD FILTER is CAK.

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Related Devices (Code: CAK)

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K061103HAEMONETICS 40U RBC FILTER BAGHaemonetics Corp.K022477SUMMIT MEDICAL LTD TRANSFUSION FILTER, MODEL LF400 & SUMMIT MEDICAL LTD TRANSFUSION FILTER WITH ADMINISTRATION SETSummit Medical , Ltd.K990310CHARTER MEDICAL, LTD MP 450 (40 MICRON FILTER)Charter Medical, Ltd.K982822FENWAL 20 MICRON PEDIATRIC TRANSFUSION FILTER MODEL 4C7701, FENWAL 20 MICRON PEDIATRIC TRANSFUSION FILTER SET MODEL 4C72Baxter Healthcare CorpK972159FENWAL 40 MICRON TRANSFUSION FILTERBaxter Healthcare CorpK970225ALPHA MICRON 20/40 MICROAGGREGATE FILTERAlpha Therapeutic Corp.

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.

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