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FDA 510(k)

MERRITTAN SUN SYSTEM

K-Number: K834488 · 1984-02-09

Decision Date1984-02-09
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MERRITTAN SUN SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Interfit A.G. Dba/Int'L Tanning Sys. It received FDA 510(k) clearance on 1984-02-09 under 510(k) number K834488. 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 MERRITTAN SUN SYSTEM?

MERRITTAN SUN SYSTEM is a medical device that received FDA 510(k) clearance on 1984-02-09. The listed applicant is Interfit A.G. Dba/Int'L Tanning Sys. The 510(k) number is K834488.

When did MERRITTAN SUN SYSTEM receive FDA 510(k) clearance?

MERRITTAN SUN SYSTEM received FDA 510(k) clearance on 1984-02-09, under 510(k) number K834488.

Who is the listed applicant for MERRITTAN SUN SYSTEM?

The FDA 510(k) record lists Interfit A.G. Dba/Int'L Tanning Sys as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MERRITTAN SUN SYSTEM?

The FDA product code for MERRITTAN SUN SYSTEM 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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