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FDA 510(k)

CHOLANGIOGRAM CATHETER KIT

K-Number: K920236 · 1992-05-06

Decision Date1992-05-06
Product CodeFGE
Advisory CommitteeGU
DecisionUnknown

Device Summary

CHOLANGIOGRAM CATHETER KIT is the device name listed in this FDA 510(k) record. The listed applicant is Mccol Medical,Inc.. It received FDA 510(k) clearance on 1992-05-06 under 510(k) number K920236. The device is classified under product code FGE. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the CHOLANGIOGRAM CATHETER KIT?

CHOLANGIOGRAM CATHETER KIT is a medical device that received FDA 510(k) clearance on 1992-05-06. The listed applicant is Mccol Medical,Inc.. The 510(k) number is K920236.

When did CHOLANGIOGRAM CATHETER KIT receive FDA 510(k) clearance?

CHOLANGIOGRAM CATHETER KIT received FDA 510(k) clearance on 1992-05-06, under 510(k) number K920236.

Who is the listed applicant for CHOLANGIOGRAM CATHETER KIT?

The FDA 510(k) record lists Mccol Medical,Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHOLANGIOGRAM CATHETER KIT?

The FDA product code for CHOLANGIOGRAM CATHETER KIT 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.

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

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