INTERGARD WOVEN COLLAGEN COATED VASCULAR PROSTHESES
K-Number: K970843 · 1997-06-05
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Device Summary
Frequently Asked Questions
What is the INTERGARD WOVEN COLLAGEN COATED VASCULAR PROSTHESES?
INTERGARD WOVEN COLLAGEN COATED VASCULAR PROSTHESES is a medical device that received FDA 510(k) clearance on 1997-06-05. The listed applicant is Intervascular, Inc.. The 510(k) number is K970843.
When did INTERGARD WOVEN COLLAGEN COATED VASCULAR PROSTHESES receive FDA 510(k) clearance?
INTERGARD WOVEN COLLAGEN COATED VASCULAR PROSTHESES received FDA 510(k) clearance on 1997-06-05, under 510(k) number K970843.
Who is the listed applicant for INTERGARD WOVEN COLLAGEN COATED VASCULAR PROSTHESES?
The FDA 510(k) record lists Intervascular, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INTERGARD WOVEN COLLAGEN COATED VASCULAR PROSTHESES?
The FDA product code for INTERGARD WOVEN COLLAGEN COATED VASCULAR PROSTHESES is DSY.
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.
Other records listing Intervascular, Inc. as applicant
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: DSY)
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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