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FDA 510(k)

FREE SUN PRO DESIGN 3000 AND 3800

K-Number: K925171 · 1992-12-29

ApplicantFree Sun Prod. AB
Decision Date1992-12-29
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FREE SUN PRO DESIGN 3000 AND 3800 is the device name listed in this FDA 510(k) record. The listed applicant is Free Sun Prod. AB. It received FDA 510(k) clearance on 1992-12-29 under 510(k) number K925171. 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 FREE SUN PRO DESIGN 3000 AND 3800?

FREE SUN PRO DESIGN 3000 AND 3800 is a medical device that received FDA 510(k) clearance on 1992-12-29. The listed applicant is Free Sun Prod. AB. The 510(k) number is K925171.

When did FREE SUN PRO DESIGN 3000 AND 3800 receive FDA 510(k) clearance?

FREE SUN PRO DESIGN 3000 AND 3800 received FDA 510(k) clearance on 1992-12-29, under 510(k) number K925171.

Who is the listed applicant for FREE SUN PRO DESIGN 3000 AND 3800?

The FDA 510(k) record lists Free Sun Prod. AB as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FREE SUN PRO DESIGN 3000 AND 3800?

The FDA product code for FREE SUN PRO DESIGN 3000 AND 3800 is FTC.

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Related Devices (Code: FTC)

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Official Source

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