ANGIOMED PERCUTANEOUS TRANSHEPATIC CHOLANGIOGTAPHY
K-Number: K855142 · 1986-03-11
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Device Summary
Frequently Asked Questions
What is the ANGIOMED PERCUTANEOUS TRANSHEPATIC CHOLANGIOGTAPHY?
ANGIOMED PERCUTANEOUS TRANSHEPATIC CHOLANGIOGTAPHY is a medical device that received FDA 510(k) clearance on 1986-03-11. The listed applicant is Angiomed U.S., Inc.. The 510(k) number is K855142.
When did ANGIOMED PERCUTANEOUS TRANSHEPATIC CHOLANGIOGTAPHY receive FDA 510(k) clearance?
ANGIOMED PERCUTANEOUS TRANSHEPATIC CHOLANGIOGTAPHY received FDA 510(k) clearance on 1986-03-11, under 510(k) number K855142.
Who is the listed applicant for ANGIOMED PERCUTANEOUS TRANSHEPATIC CHOLANGIOGTAPHY?
The FDA 510(k) record lists Angiomed U.S., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANGIOMED PERCUTANEOUS TRANSHEPATIC CHOLANGIOGTAPHY?
The FDA product code for ANGIOMED PERCUTANEOUS TRANSHEPATIC CHOLANGIOGTAPHY 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 Angiomed U.S., 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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