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FDA 510(k)

MODIFICATION OF SUNTANA SUN SYSTEM BED

K-Number: K861989 · 1986-06-09

ApplicantHawaiian Tan Spa
Decision Date1986-06-09
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MODIFICATION OF SUNTANA SUN SYSTEM BED is the device name listed in this FDA 510(k) record. The listed applicant is Hawaiian Tan Spa. It received FDA 510(k) clearance on 1986-06-09 under 510(k) number K861989. 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 MODIFICATION OF SUNTANA SUN SYSTEM BED?

MODIFICATION OF SUNTANA SUN SYSTEM BED is a medical device that received FDA 510(k) clearance on 1986-06-09. The listed applicant is Hawaiian Tan Spa. The 510(k) number is K861989.

When did MODIFICATION OF SUNTANA SUN SYSTEM BED receive FDA 510(k) clearance?

MODIFICATION OF SUNTANA SUN SYSTEM BED received FDA 510(k) clearance on 1986-06-09, under 510(k) number K861989.

Who is the listed applicant for MODIFICATION OF SUNTANA SUN SYSTEM BED?

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

What is the FDA product code for MODIFICATION OF SUNTANA SUN SYSTEM BED?

The FDA product code for MODIFICATION OF SUNTANA SUN SYSTEM BED is FTC.

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Related Devices (Code: FTC)

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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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