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FDA 510(k)

TANNING BED

K-Number: K883929 · 1988-10-03

Decision Date1988-10-03
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TANNING BED is the device name listed in this FDA 510(k) record. The listed applicant is Dallas Tan, Inc.. It received FDA 510(k) clearance on 1988-10-03 under 510(k) number K883929. 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 TANNING BED?

TANNING BED is a medical device that received FDA 510(k) clearance on 1988-10-03. The listed applicant is Dallas Tan, Inc.. The 510(k) number is K883929.

When did TANNING BED receive FDA 510(k) clearance?

TANNING BED received FDA 510(k) clearance on 1988-10-03, under 510(k) number K883929.

Who is the listed applicant for TANNING BED?

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

What is the FDA product code for TANNING BED?

The FDA product code for TANNING BED is FTC.

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: FTC)

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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