OPERATIVE CHOLANGIOGRAM CATHETER
K-Number: K924981 · 1993-04-06
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Device Summary
Frequently Asked Questions
What is the OPERATIVE CHOLANGIOGRAM CATHETER?
OPERATIVE CHOLANGIOGRAM CATHETER is a medical device that received FDA 510(k) clearance on 1993-04-06. The listed applicant is Taut, Inc.. The 510(k) number is K924981.
When did OPERATIVE CHOLANGIOGRAM CATHETER receive FDA 510(k) clearance?
OPERATIVE CHOLANGIOGRAM CATHETER received FDA 510(k) clearance on 1993-04-06, under 510(k) number K924981.
Who is the listed applicant for OPERATIVE CHOLANGIOGRAM CATHETER?
The FDA 510(k) record lists Taut, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OPERATIVE CHOLANGIOGRAM CATHETER?
The FDA product code for OPERATIVE CHOLANGIOGRAM CATHETER is GBZ.
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 Taut, 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: GBZ)
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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