WILTEK STANDARD CHOLANGIOGRAPHY CATHETER
K-Number: K912288 · 1991-09-23
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Device Summary
Frequently Asked Questions
What is the WILTEK STANDARD CHOLANGIOGRAPHY CATHETER?
WILTEK STANDARD CHOLANGIOGRAPHY CATHETER is a medical device that received FDA 510(k) clearance on 1991-09-23. The listed applicant is Wiltek Medical, Inc.. The 510(k) number is K912288.
When did WILTEK STANDARD CHOLANGIOGRAPHY CATHETER receive FDA 510(k) clearance?
WILTEK STANDARD CHOLANGIOGRAPHY CATHETER received FDA 510(k) clearance on 1991-09-23, under 510(k) number K912288.
Who is the listed applicant for WILTEK STANDARD CHOLANGIOGRAPHY CATHETER?
The FDA 510(k) record lists Wiltek Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WILTEK STANDARD CHOLANGIOGRAPHY CATHETER?
The FDA product code for WILTEK STANDARD CHOLANGIOGRAPHY CATHETER 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 Wiltek Medical, 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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