WALLSTENT TRANSHEPATIC BILIARY ENDOPROSTHESIS
K-Number: K982005 · 1998-09-02
Advertisement
Device Summary
Frequently Asked Questions
What is the WALLSTENT TRANSHEPATIC BILIARY ENDOPROSTHESIS?
WALLSTENT TRANSHEPATIC BILIARY ENDOPROSTHESIS is a medical device that received FDA 510(k) clearance on 1998-09-02. The listed applicant is Boston Scientific Scimed, Inc.. The 510(k) number is K982005.
When did WALLSTENT TRANSHEPATIC BILIARY ENDOPROSTHESIS receive FDA 510(k) clearance?
WALLSTENT TRANSHEPATIC BILIARY ENDOPROSTHESIS received FDA 510(k) clearance on 1998-09-02, under 510(k) number K982005.
Who is the listed applicant for WALLSTENT TRANSHEPATIC BILIARY ENDOPROSTHESIS?
The FDA 510(k) record lists Boston Scientific Scimed, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WALLSTENT TRANSHEPATIC BILIARY ENDOPROSTHESIS?
The FDA product code for WALLSTENT TRANSHEPATIC BILIARY 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 Boston Scientific Scimed, 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.
Advertisement