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FDA 510(k)

ROAD WARRIOR

K-Number: K935749 · 1995-01-13

ApplicantRedman, Inc.
Decision Date1995-01-13
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

ROAD WARRIOR is the device name listed in this FDA 510(k) record. The listed applicant is Redman, Inc.. It received FDA 510(k) clearance on 1995-01-13 under 510(k) number K935749. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the ROAD WARRIOR?

ROAD WARRIOR is a medical device that received FDA 510(k) clearance on 1995-01-13. The listed applicant is Redman, Inc.. The 510(k) number is K935749.

When did ROAD WARRIOR receive FDA 510(k) clearance?

ROAD WARRIOR received FDA 510(k) clearance on 1995-01-13, under 510(k) number K935749.

Who is the listed applicant for ROAD WARRIOR?

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

What is the FDA product code for ROAD WARRIOR?

The FDA product code for ROAD WARRIOR is ITI.

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Other records listing Redman, Inc. as applicant

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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Related Devices (Code: ITI)

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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