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FDA 510(k)

BELZER UW-CSS

K-Number: K883782 · 1989-04-20

ApplicantDu Pont Critical Care
Decision Date1989-04-20
Product CodeKDL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BELZER UW-CSS is the device name listed in this FDA 510(k) record. The listed applicant is Du Pont Critical Care. It received FDA 510(k) clearance on 1989-04-20 under 510(k) number K883782. The device is classified under product code KDL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BELZER UW-CSS?

BELZER UW-CSS is a medical device that received FDA 510(k) clearance on 1989-04-20. The listed applicant is Du Pont Critical Care. The 510(k) number is K883782.

When did BELZER UW-CSS receive FDA 510(k) clearance?

BELZER UW-CSS received FDA 510(k) clearance on 1989-04-20, under 510(k) number K883782.

Who is the listed applicant for BELZER UW-CSS?

The FDA 510(k) record lists Du Pont Critical Care as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BELZER UW-CSS?

The FDA product code for BELZER UW-CSS is KDL.

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Related Devices (Code: KDL)

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.

K241239OrganProtex HTK SolutionBridge TO Life, Ltd.K221386PERF-GEN Pulsatile Perfusion SolutionInstitut Georges LopezK221387BEL-GEN Cold Storage SolutionInstitut Georges LopezK211842Servator M SALF SolutionS.A.L.F. SpaK192408Custodiol HTK SolutionDr. Franz Kohler Chemie GmbHK170150Servator H SALF solution-1000 ml PVC free bags, Servator H SALF solution-2000 ml PVC free bagsS.A.L.F. Spa

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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