USCI ENDOPROSTHESIS
K-Number: K834574 · 1984-04-05
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Device Summary
Frequently Asked Questions
What is the USCI ENDOPROSTHESIS?
USCI ENDOPROSTHESIS is a medical device that received FDA 510(k) clearance on 1984-04-05. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K834574.
When did USCI ENDOPROSTHESIS receive FDA 510(k) clearance?
USCI ENDOPROSTHESIS received FDA 510(k) clearance on 1984-04-05, under 510(k) number K834574.
Who is the listed applicant for USCI ENDOPROSTHESIS?
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 USCI ENDOPROSTHESIS?
The FDA product code for USCI ENDOPROSTHESIS 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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