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FDA 510(k)

WILSON-COOK ESOPHAGEAL MOTILITY CATHETER

K-Number: K900239 · 1990-07-16

ApplicantWilson-Cook Medical, Inc.
Decision Date1990-07-16
Product CodeKLA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

WILSON-COOK ESOPHAGEAL MOTILITY CATHETER 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 1990-07-16 under 510(k) number K900239. The device is classified under product code KLA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WILSON-COOK ESOPHAGEAL MOTILITY CATHETER?

WILSON-COOK ESOPHAGEAL MOTILITY CATHETER is a medical device that received FDA 510(k) clearance on 1990-07-16. The listed applicant is Wilson-Cook Medical, Inc.. The 510(k) number is K900239.

When did WILSON-COOK ESOPHAGEAL MOTILITY CATHETER receive FDA 510(k) clearance?

WILSON-COOK ESOPHAGEAL MOTILITY CATHETER received FDA 510(k) clearance on 1990-07-16, under 510(k) number K900239.

Who is the listed applicant for WILSON-COOK ESOPHAGEAL MOTILITY CATHETER?

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 WILSON-COOK ESOPHAGEAL MOTILITY CATHETER?

The FDA product code for WILSON-COOK ESOPHAGEAL MOTILITY CATHETER is KLA.

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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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