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FDA 510(k)

HOPE MODEL 126, AUTO/PROCES., DEN. FLM

K-Number: K800134 · 1980-05-02

ApplicantHope Industries, Inc.
Decision Date1980-05-02
Product CodeIWZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

HOPE MODEL 126, AUTO/PROCES., DEN. FLM is the device name listed in this FDA 510(k) record. The listed applicant is Hope Industries, Inc.. It received FDA 510(k) clearance on 1980-05-02 under 510(k) number K800134. The device is classified under product code IWZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOPE MODEL 126, AUTO/PROCES., DEN. FLM?

HOPE MODEL 126, AUTO/PROCES., DEN. FLM is a medical device that received FDA 510(k) clearance on 1980-05-02. The listed applicant is Hope Industries, Inc.. The 510(k) number is K800134.

When did HOPE MODEL 126, AUTO/PROCES., DEN. FLM receive FDA 510(k) clearance?

HOPE MODEL 126, AUTO/PROCES., DEN. FLM received FDA 510(k) clearance on 1980-05-02, under 510(k) number K800134.

Who is the listed applicant for HOPE MODEL 126, AUTO/PROCES., DEN. FLM?

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

What is the FDA product code for HOPE MODEL 126, AUTO/PROCES., DEN. FLM?

The FDA product code for HOPE MODEL 126, AUTO/PROCES., DEN. FLM is IWZ.

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Related Devices (Code: IWZ)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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