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FDA 510(k)

SUNBED/CANOPY, MODELS GTI 24N,30R,30RE & 37RE

K-Number: K860509 · 1986-03-05

ApplicantEcomatic GmbH, Frankfurt, F.R.G.
Decision Date1986-03-05
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SUNBED/CANOPY, MODELS GTI 24N,30R,30RE & 37RE is the device name listed in this FDA 510(k) record. The listed applicant is Ecomatic GmbH, Frankfurt, F.R.G.. It received FDA 510(k) clearance on 1986-03-05 under 510(k) number K860509. 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 SUNBED/CANOPY, MODELS GTI 24N,30R,30RE & 37RE?

SUNBED/CANOPY, MODELS GTI 24N,30R,30RE & 37RE is a medical device that received FDA 510(k) clearance on 1986-03-05. The listed applicant is Ecomatic GmbH, Frankfurt, F.R.G.. The 510(k) number is K860509.

When did SUNBED/CANOPY, MODELS GTI 24N,30R,30RE & 37RE receive FDA 510(k) clearance?

SUNBED/CANOPY, MODELS GTI 24N,30R,30RE & 37RE received FDA 510(k) clearance on 1986-03-05, under 510(k) number K860509.

Who is the listed applicant for SUNBED/CANOPY, MODELS GTI 24N,30R,30RE & 37RE?

The FDA 510(k) record lists Ecomatic GmbH, Frankfurt, F.R.G. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUNBED/CANOPY, MODELS GTI 24N,30R,30RE & 37RE?

The FDA product code for SUNBED/CANOPY, MODELS GTI 24N,30R,30RE & 37RE is 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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