FDA 510(k)

ULTRASUN 4000 FT & 15000-8 SUNTANNING UNIT

K-Number: K860929 · 1986-03-28

ApplicantMedical Device Consultants, Inc.

Decision Date1986-03-28

Product CodeFTC

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

ULTRASUN 4000 FT & 15000-8 SUNTANNING UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Consultants, Inc.. It received FDA 510(k) clearance on 1986-03-28 under 510(k) number K860929. 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 ULTRASUN 4000 FT & 15000-8 SUNTANNING UNIT?

ULTRASUN 4000 FT & 15000-8 SUNTANNING UNIT is a medical device that received FDA 510(k) clearance on 1986-03-28. The listed applicant is Medical Device Consultants, Inc.. The 510(k) number is K860929.

When did ULTRASUN 4000 FT & 15000-8 SUNTANNING UNIT receive FDA 510(k) clearance?

ULTRASUN 4000 FT & 15000-8 SUNTANNING UNIT received FDA 510(k) clearance on 1986-03-28, under 510(k) number K860929.

Who is the listed applicant for ULTRASUN 4000 FT & 15000-8 SUNTANNING UNIT?

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

What is the FDA product code for ULTRASUN 4000 FT & 15000-8 SUNTANNING UNIT?

The FDA product code for ULTRASUN 4000 FT & 15000-8 SUNTANNING UNIT is FTC.

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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.