VIASPAN (BELZER UW - CSS)
K-Number: K944866 · 1996-04-22
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Device Summary
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
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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