GUIDANT MEGALINK BILIARY STENT, MODEL FG1002949-58
K-Number: K991032 · 1999-04-30
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Device Summary
Frequently Asked Questions
What is the GUIDANT MEGALINK BILIARY STENT, MODEL FG1002949-58?
GUIDANT MEGALINK BILIARY STENT, MODEL FG1002949-58 is a medical device that received FDA 510(k) clearance on 1999-04-30. The listed applicant is Guidant Corp.. The 510(k) number is K991032.
When did GUIDANT MEGALINK BILIARY STENT, MODEL FG1002949-58 receive FDA 510(k) clearance?
GUIDANT MEGALINK BILIARY STENT, MODEL FG1002949-58 received FDA 510(k) clearance on 1999-04-30, under 510(k) number K991032.
Who is the listed applicant for GUIDANT MEGALINK BILIARY STENT, MODEL FG1002949-58?
The FDA 510(k) record lists Guidant Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GUIDANT MEGALINK BILIARY STENT, MODEL FG1002949-58?
The FDA product code for GUIDANT MEGALINK BILIARY STENT, MODEL FG1002949-58 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 Guidant Corp. 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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