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FDA 510(k)

SUN-DREAMER SUNTANNING BED

K-Number: K862142 · 1986-06-17

Decision Date1986-06-17
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SUN-DREAMER SUNTANNING BED is the device name listed in this FDA 510(k) record. The listed applicant is Sun-Dream Tanning , Ltd.. It received FDA 510(k) clearance on 1986-06-17 under 510(k) number K862142. 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 SUN-DREAMER SUNTANNING BED?

SUN-DREAMER SUNTANNING BED is a medical device that received FDA 510(k) clearance on 1986-06-17. The listed applicant is Sun-Dream Tanning , Ltd.. The 510(k) number is K862142.

When did SUN-DREAMER SUNTANNING BED receive FDA 510(k) clearance?

SUN-DREAMER SUNTANNING BED received FDA 510(k) clearance on 1986-06-17, under 510(k) number K862142.

Who is the listed applicant for SUN-DREAMER SUNTANNING BED?

The FDA 510(k) record lists Sun-Dream Tanning , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUN-DREAMER SUNTANNING BED?

The FDA product code for SUN-DREAMER SUNTANNING 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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