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FDA 510(k)

CHIEF SR

K-Number: K940919 · 1995-02-03

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

Device Summary

CHIEF SR 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 K940919. The device is classified under product code IPL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the CHIEF SR?

CHIEF SR 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 K940919.

When did CHIEF SR receive FDA 510(k) clearance?

CHIEF SR received FDA 510(k) clearance on 1995-02-03, under 510(k) number K940919.

Who is the listed applicant for CHIEF SR?

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 CHIEF SR?

The FDA product code for CHIEF SR is IPL.

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Other records listing Redman, Inc. as applicant

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Related Devices (Code: IPL)

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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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