CLARUS CHOLANGIOGRAM CATHETER KIT
K-Number: K925742 · 1993-06-01
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Device Summary
Frequently Asked Questions
What is the CLARUS CHOLANGIOGRAM CATHETER KIT?
CLARUS CHOLANGIOGRAM CATHETER KIT is a medical device that received FDA 510(k) clearance on 1993-06-01. The listed applicant is Clarus Medical Systems, Inc.. The 510(k) number is K925742.
When did CLARUS CHOLANGIOGRAM CATHETER KIT receive FDA 510(k) clearance?
CLARUS CHOLANGIOGRAM CATHETER KIT received FDA 510(k) clearance on 1993-06-01, under 510(k) number K925742.
Who is the listed applicant for CLARUS CHOLANGIOGRAM CATHETER KIT?
The FDA 510(k) record lists Clarus Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CLARUS CHOLANGIOGRAM CATHETER KIT?
The FDA product code for CLARUS CHOLANGIOGRAM CATHETER KIT 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 Clarus Medical 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: 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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