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FDA 510(k)

ERCP CATHETER, HYDROPHILIC COATED

K-Number: K932205 · 1994-01-03

ApplicantWilson-Cook Medical, Inc.
Decision Date1994-01-03
Product CodeGBX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ERCP CATHETER, HYDROPHILIC COATED is the device name listed in this FDA 510(k) record. The listed applicant is Wilson-Cook Medical, Inc.. It received FDA 510(k) clearance on 1994-01-03 under 510(k) number K932205. The device is classified under product code GBX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ERCP CATHETER, HYDROPHILIC COATED?

ERCP CATHETER, HYDROPHILIC COATED is a medical device that received FDA 510(k) clearance on 1994-01-03. The listed applicant is Wilson-Cook Medical, Inc.. The 510(k) number is K932205.

When did ERCP CATHETER, HYDROPHILIC COATED receive FDA 510(k) clearance?

ERCP CATHETER, HYDROPHILIC COATED received FDA 510(k) clearance on 1994-01-03, under 510(k) number K932205.

Who is the listed applicant for ERCP CATHETER, HYDROPHILIC COATED?

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

What is the FDA product code for ERCP CATHETER, HYDROPHILIC COATED?

The FDA product code for ERCP CATHETER, HYDROPHILIC COATED is GBX.

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Related Devices (Code: GBX)

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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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