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FDA 510(k)

GENERAL EQUIPMENT COVER

K-Number: K782155 · 1979-01-17

ApplicantContour Fabricators, Inc.
Decision Date1979-01-17
Product CodeIZL
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

GENERAL EQUIPMENT COVER is the device name listed in this FDA 510(k) record. The listed applicant is Contour Fabricators, Inc.. It received FDA 510(k) clearance on 1979-01-17 under 510(k) number K782155. The device is classified under product code IZL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GENERAL EQUIPMENT COVER?

GENERAL EQUIPMENT COVER is a medical device that received FDA 510(k) clearance on 1979-01-17. The listed applicant is Contour Fabricators, Inc.. The 510(k) number is K782155.

When did GENERAL EQUIPMENT COVER receive FDA 510(k) clearance?

GENERAL EQUIPMENT COVER received FDA 510(k) clearance on 1979-01-17, under 510(k) number K782155.

Who is the listed applicant for GENERAL EQUIPMENT COVER?

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

What is the FDA product code for GENERAL EQUIPMENT COVER?

The FDA product code for GENERAL EQUIPMENT COVER is IZL.

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Other records listing Contour Fabricators, Inc. as applicant

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Related Devices (Code: IZL)

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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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