RADIALLY-SUPPORTED VASCULAR PROSTHESES
K-Number: K870884 · 1988-02-05
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Device Summary
Frequently Asked Questions
What is the RADIALLY-SUPPORTED VASCULAR PROSTHESES?
RADIALLY-SUPPORTED VASCULAR PROSTHESES is a medical device that received FDA 510(k) clearance on 1988-02-05. The listed applicant is Intervascular, Inc.. The 510(k) number is K870884.
When did RADIALLY-SUPPORTED VASCULAR PROSTHESES receive FDA 510(k) clearance?
RADIALLY-SUPPORTED VASCULAR PROSTHESES received FDA 510(k) clearance on 1988-02-05, under 510(k) number K870884.
Who is the listed applicant for RADIALLY-SUPPORTED 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 RADIALLY-SUPPORTED VASCULAR PROSTHESES?
The FDA product code for RADIALLY-SUPPORTED 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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