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FDA 510(k)

VIASPAN (BELZER UW - CSS)

K-Number: K944866 · 1996-04-22

Decision Date1996-04-22
Product CodeKDL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VIASPAN (BELZER UW - CSS) is the device name listed in this FDA 510(k) record. The listed applicant is The Dupont Merck Pharmaceutical Co.. It received FDA 510(k) clearance on 1996-04-22 under 510(k) number K944866. 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 VIASPAN (BELZER UW - CSS)?

VIASPAN (BELZER UW - CSS) is a medical device that received FDA 510(k) clearance on 1996-04-22. The listed applicant is The Dupont Merck Pharmaceutical Co.. The 510(k) number is K944866.

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

VIASPAN (BELZER UW - CSS) received FDA 510(k) clearance on 1996-04-22, under 510(k) number K944866.

Who is the listed applicant for VIASPAN (BELZER UW - CSS)?

The FDA 510(k) record lists The Dupont Merck Pharmaceutical Co. as the applicant. This does not by itself establish the device manufacturer.

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

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

Related Clinical Trials

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.

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.

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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