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FDA 510(k)

UV-A SUNTANNING EQUIPMENT 1000-8000

K-Number: K834495 · 1984-02-06

ApplicantFuturen, Inc.
Decision Date1984-02-06
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

UV-A SUNTANNING EQUIPMENT 1000-8000 is the device name listed in this FDA 510(k) record. The listed applicant is Futuren, Inc.. It received FDA 510(k) clearance on 1984-02-06 under 510(k) number K834495. 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 UV-A SUNTANNING EQUIPMENT 1000-8000?

UV-A SUNTANNING EQUIPMENT 1000-8000 is a medical device that received FDA 510(k) clearance on 1984-02-06. The listed applicant is Futuren, Inc.. The 510(k) number is K834495.

When did UV-A SUNTANNING EQUIPMENT 1000-8000 receive FDA 510(k) clearance?

UV-A SUNTANNING EQUIPMENT 1000-8000 received FDA 510(k) clearance on 1984-02-06, under 510(k) number K834495.

Who is the listed applicant for UV-A SUNTANNING EQUIPMENT 1000-8000?

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

What is the FDA product code for UV-A SUNTANNING EQUIPMENT 1000-8000?

The FDA product code for UV-A SUNTANNING EQUIPMENT 1000-8000 is FTC.

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Related Devices (Code: FTC)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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