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FDA 510(k)

SUN VALLEY TANS

K-Number: K801543 · 1980-09-16

Decision Date1980-09-16
Product CodeLEJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SUN VALLEY TANS is the device name listed in this FDA 510(k) record. The listed applicant is Sun Valley Tans, Inc.. It received FDA 510(k) clearance on 1980-09-16 under 510(k) number K801543. 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 VALLEY TANS?

SUN VALLEY TANS is a medical device that received FDA 510(k) clearance on 1980-09-16. The listed applicant is Sun Valley Tans, Inc.. The 510(k) number is K801543.

When did SUN VALLEY TANS receive FDA 510(k) clearance?

SUN VALLEY TANS received FDA 510(k) clearance on 1980-09-16, under 510(k) number K801543.

Who is the listed applicant for SUN VALLEY TANS?

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

What is the FDA product code for SUN VALLEY TANS?

The FDA product code for SUN VALLEY TANS is LEJ.

Related Clinical Trials

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.

Related Devices (Code: LEJ)

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.

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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