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FDA 510(k)

REDOX

K-Number: K953850 · 1996-03-04

ApplicantKinetic Concepts, Inc.
Decision Date1996-03-04
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

REDOX 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 1996-03-04 under 510(k) number K953850. 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 REDOX?

REDOX is a medical device that received FDA 510(k) clearance on 1996-03-04. The listed applicant is Kinetic Concepts, Inc.. The 510(k) number is K953850.

When did REDOX receive FDA 510(k) clearance?

REDOX received FDA 510(k) clearance on 1996-03-04, under 510(k) number K953850.

Who is the listed applicant for REDOX?

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 REDOX?

The FDA product code for REDOX 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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