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FDA 510(k)

THE SUNFACTORY

K-Number: K810688 · 1981-04-23

ApplicantWesgold Marketing, Inc.
Decision Date1981-04-23
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

THE SUNFACTORY is the device name listed in this FDA 510(k) record. The listed applicant is Wesgold Marketing, Inc.. It received FDA 510(k) clearance on 1981-04-23 under 510(k) number K810688. The device is classified under product code FTC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE SUNFACTORY?

THE SUNFACTORY is a medical device that received FDA 510(k) clearance on 1981-04-23. The listed applicant is Wesgold Marketing, Inc.. The 510(k) number is K810688.

When did THE SUNFACTORY receive FDA 510(k) clearance?

THE SUNFACTORY received FDA 510(k) clearance on 1981-04-23, under 510(k) number K810688.

Who is the listed applicant for THE SUNFACTORY?

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

What is the FDA product code for THE SUNFACTORY?

The FDA product code for THE SUNFACTORY is FTC.

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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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