BILIARY BALLOON DILATOR
K-Number: K901432 · 1990-06-21
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Device Summary
Frequently Asked Questions
What is the BILIARY BALLOON DILATOR?
BILIARY BALLOON DILATOR is a medical device that received FDA 510(k) clearance on 1990-06-21. The listed applicant is Telemed Systems, Inc.. The 510(k) number is K901432.
When did BILIARY BALLOON DILATOR receive FDA 510(k) clearance?
BILIARY BALLOON DILATOR received FDA 510(k) clearance on 1990-06-21, under 510(k) number K901432.
Who is the listed applicant for BILIARY BALLOON DILATOR?
The FDA 510(k) record lists Telemed Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BILIARY BALLOON DILATOR?
The FDA product code for BILIARY BALLOON DILATOR 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 Telemed Systems, 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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