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FDA 510(k)

CLARUS CHOLANGIOGRAM CATHETER KIT

K-Number: K925742 · 1993-06-01

Decision Date1993-06-01
Product CodeGBZ
Advisory CommitteeSU
DecisionUnknown

Device Summary

CLARUS CHOLANGIOGRAM CATHETER KIT is the device name listed in this FDA 510(k) record. The listed applicant is Clarus Medical Systems, Inc.. It received FDA 510(k) clearance on 1993-06-01 under 510(k) number K925742. The device is classified under product code GBZ. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

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.

View all 22 devices →

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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