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FDA 510(k)

COWBOY III

K-Number: K932215 · 1993-07-21

ApplicantKinetic Concepts, Inc.
Decision Date1993-07-21
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

COWBOY III is the device name listed in this FDA 510(k) record. The listed applicant is Kinetic Concepts, Inc.. It received FDA 510(k) clearance on 1993-07-21 under 510(k) number K932215. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COWBOY III?

COWBOY III is a medical device that received FDA 510(k) clearance on 1993-07-21. The listed applicant is Kinetic Concepts, Inc.. The 510(k) number is K932215.

When did COWBOY III receive FDA 510(k) clearance?

COWBOY III received FDA 510(k) clearance on 1993-07-21, under 510(k) number K932215.

Who is the listed applicant for COWBOY III?

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

What is the FDA product code for COWBOY III?

The FDA product code for COWBOY III is JOW.

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Other records listing Kinetic Concepts, Inc. as applicant

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Related Devices (Code: JOW)

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.

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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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