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FDA 510(k)

SUNTANNING EQUIPMENT

K-Number: K851532 · 1985-05-07

ApplicantOakport Intl., Inc.
Decision Date1985-05-07
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SUNTANNING EQUIPMENT is the device name listed in this FDA 510(k) record. The listed applicant is Oakport Intl., Inc.. It received FDA 510(k) clearance on 1985-05-07 under 510(k) number K851532. 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 SUNTANNING EQUIPMENT?

SUNTANNING EQUIPMENT is a medical device that received FDA 510(k) clearance on 1985-05-07. The listed applicant is Oakport Intl., Inc.. The 510(k) number is K851532.

When did SUNTANNING EQUIPMENT receive FDA 510(k) clearance?

SUNTANNING EQUIPMENT received FDA 510(k) clearance on 1985-05-07, under 510(k) number K851532.

Who is the listed applicant for SUNTANNING EQUIPMENT?

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

What is the FDA product code for SUNTANNING EQUIPMENT?

The FDA product code for SUNTANNING EQUIPMENT 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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