BILIARY INDWELLING STENT
K-Number: K834351 · 1984-03-22
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Device Summary
Frequently Asked Questions
What is the BILIARY INDWELLING STENT?
BILIARY INDWELLING STENT is a medical device that received FDA 510(k) clearance on 1984-03-22. The listed applicant is Hobbs Medical, Inc.. The 510(k) number is K834351.
When did BILIARY INDWELLING STENT receive FDA 510(k) clearance?
BILIARY INDWELLING STENT received FDA 510(k) clearance on 1984-03-22, under 510(k) number K834351.
Who is the listed applicant for BILIARY INDWELLING STENT?
The FDA 510(k) record lists Hobbs Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BILIARY INDWELLING STENT?
The FDA product code for BILIARY INDWELLING STENT 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 Hobbs Medical, 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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