BARD/ANGIOMED STENTS
K-Number: K896391 · 1990-03-29
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Device Summary
Frequently Asked Questions
What is the BARD/ANGIOMED STENTS?
BARD/ANGIOMED STENTS is a medical device that received FDA 510(k) clearance on 1990-03-29. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K896391.
When did BARD/ANGIOMED STENTS receive FDA 510(k) clearance?
BARD/ANGIOMED STENTS received FDA 510(k) clearance on 1990-03-29, under 510(k) number K896391.
Who is the listed applicant for BARD/ANGIOMED STENTS?
The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BARD/ANGIOMED STENTS?
The FDA product code for BARD/ANGIOMED STENTS is FGE.
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 C.R. Bard, 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: FGE)
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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