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FDA 510(k)

SEMI-OVAL MODULAR SUNTANNING BOOTH

K-Number: K802756 · 1981-01-22

ApplicantTannhut
Decision Date1981-01-22
Product CodeLEJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SEMI-OVAL MODULAR SUNTANNING BOOTH is the device name listed in this FDA 510(k) record. The listed applicant is Tannhut. It received FDA 510(k) clearance on 1981-01-22 under 510(k) number K802756. 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 SEMI-OVAL MODULAR SUNTANNING BOOTH?

SEMI-OVAL MODULAR SUNTANNING BOOTH is a medical device that received FDA 510(k) clearance on 1981-01-22. The listed applicant is Tannhut. The 510(k) number is K802756.

When did SEMI-OVAL MODULAR SUNTANNING BOOTH receive FDA 510(k) clearance?

SEMI-OVAL MODULAR SUNTANNING BOOTH received FDA 510(k) clearance on 1981-01-22, under 510(k) number K802756.

Who is the listed applicant for SEMI-OVAL MODULAR SUNTANNING BOOTH?

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

What is the FDA product code for SEMI-OVAL MODULAR SUNTANNING BOOTH?

The FDA product code for SEMI-OVAL MODULAR SUNTANNING BOOTH 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.

Other records listing Tannhut as applicant

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.

View all 7 devices →

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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