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FDA 510(k)

PHASE V-MODEL 1500 RUVA

K-Number: K854131 · 1985-11-08

ApplicantApollo'S Suntanning Supplies
Decision Date1985-11-08
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PHASE V-MODEL 1500 RUVA is the device name listed in this FDA 510(k) record. The listed applicant is Apollo'S Suntanning Supplies. It received FDA 510(k) clearance on 1985-11-08 under 510(k) number K854131. 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 PHASE V-MODEL 1500 RUVA?

PHASE V-MODEL 1500 RUVA is a medical device that received FDA 510(k) clearance on 1985-11-08. The listed applicant is Apollo'S Suntanning Supplies. The 510(k) number is K854131.

When did PHASE V-MODEL 1500 RUVA receive FDA 510(k) clearance?

PHASE V-MODEL 1500 RUVA received FDA 510(k) clearance on 1985-11-08, under 510(k) number K854131.

Who is the listed applicant for PHASE V-MODEL 1500 RUVA?

The FDA 510(k) record lists Apollo'S Suntanning Supplies as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PHASE V-MODEL 1500 RUVA?

The FDA product code for PHASE V-MODEL 1500 RUVA is FTC.

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Related Devices (Code: FTC)

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Official Source

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