UMI PERCUTANEOUS TRANSHEPATIC CHOLAN
K-Number: K833937 · 1984-01-03
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Device Summary
Frequently Asked Questions
What is the UMI PERCUTANEOUS TRANSHEPATIC CHOLAN?
UMI PERCUTANEOUS TRANSHEPATIC CHOLAN is a medical device that received FDA 510(k) clearance on 1984-01-03. The listed applicant is Universal Medical Instrument Corp.. The 510(k) number is K833937.
When did UMI PERCUTANEOUS TRANSHEPATIC CHOLAN receive FDA 510(k) clearance?
UMI PERCUTANEOUS TRANSHEPATIC CHOLAN received FDA 510(k) clearance on 1984-01-03, under 510(k) number K833937.
Who is the listed applicant for UMI PERCUTANEOUS TRANSHEPATIC CHOLAN?
The FDA 510(k) record lists Universal Medical Instrument Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UMI PERCUTANEOUS TRANSHEPATIC CHOLAN?
The FDA product code for UMI PERCUTANEOUS TRANSHEPATIC CHOLAN 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 Universal Medical Instrument 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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