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FDA 510(k)

TAN YEAR ROUND SUN BED

K-Number: K801341 · 1980-07-21

ApplicantTan-Year Round, Inc.
Decision Date1980-07-21
Product CodeLEJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TAN YEAR ROUND SUN BED is the device name listed in this FDA 510(k) record. The listed applicant is Tan-Year Round, Inc.. It received FDA 510(k) clearance on 1980-07-21 under 510(k) number K801341. The device is classified under product code LEJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TAN YEAR ROUND SUN BED?

TAN YEAR ROUND SUN BED is a medical device that received FDA 510(k) clearance on 1980-07-21. The listed applicant is Tan-Year Round, Inc.. The 510(k) number is K801341.

When did TAN YEAR ROUND SUN BED receive FDA 510(k) clearance?

TAN YEAR ROUND SUN BED received FDA 510(k) clearance on 1980-07-21, under 510(k) number K801341.

Who is the listed applicant for TAN YEAR ROUND SUN BED?

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

What is the FDA product code for TAN YEAR ROUND SUN BED?

The FDA product code for TAN YEAR ROUND SUN BED is LEJ.

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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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