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FDA 510(k)

ROAD SAVAGE

K-Number: K940920 · 1995-02-03

ApplicantRedman, Inc.
Decision Date1995-02-03
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

ROAD SAVAGE is the device name listed in this FDA 510(k) record. The listed applicant is Redman, Inc.. It received FDA 510(k) clearance on 1995-02-03 under 510(k) number K940920. 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 SAVAGE?

ROAD SAVAGE is a medical device that received FDA 510(k) clearance on 1995-02-03. The listed applicant is Redman, Inc.. The 510(k) number is K940920.

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

ROAD SAVAGE received FDA 510(k) clearance on 1995-02-03, under 510(k) number K940920.

Who is the listed applicant for ROAD SAVAGE?

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 SAVAGE?

The FDA product code for ROAD SAVAGE is ITI.

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Related Devices (Code: ITI)

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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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