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FDA 510(k)

ALISUN SUNTANNING BED

K-Number: K896831 · 1989-12-27

Decision Date1989-12-27
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ALISUN SUNTANNING BED is the device name listed in this FDA 510(k) record. The listed applicant is Alisun America, Ltd.. It received FDA 510(k) clearance on 1989-12-27 under 510(k) number K896831. 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 ALISUN SUNTANNING BED?

ALISUN SUNTANNING BED is a medical device that received FDA 510(k) clearance on 1989-12-27. The listed applicant is Alisun America, Ltd.. The 510(k) number is K896831.

When did ALISUN SUNTANNING BED receive FDA 510(k) clearance?

ALISUN SUNTANNING BED received FDA 510(k) clearance on 1989-12-27, under 510(k) number K896831.

Who is the listed applicant for ALISUN SUNTANNING BED?

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

What is the FDA product code for ALISUN SUNTANNING BED?

The FDA product code for ALISUN 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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