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FDA 510(k)

SUN ROOM TANNING BOOTH

K-Number: K801674 · 1980-09-16

ApplicantSun Tan Enterprises, Inc.
Decision Date1980-09-16
Product CodeLEJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SUN ROOM TANNING BOOTH is the device name listed in this FDA 510(k) record. The listed applicant is Sun Tan Enterprises, Inc.. It received FDA 510(k) clearance on 1980-09-16 under 510(k) number K801674. 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 SUN ROOM TANNING BOOTH?

SUN ROOM TANNING BOOTH is a medical device that received FDA 510(k) clearance on 1980-09-16. The listed applicant is Sun Tan Enterprises, Inc.. The 510(k) number is K801674.

When did SUN ROOM TANNING BOOTH receive FDA 510(k) clearance?

SUN ROOM TANNING BOOTH received FDA 510(k) clearance on 1980-09-16, under 510(k) number K801674.

Who is the listed applicant for SUN ROOM TANNING BOOTH?

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

What is the FDA product code for SUN ROOM TANNING BOOTH?

The FDA product code for SUN ROOM TANNING BOOTH 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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