FDA 510(k)

MODELS EUROSUN 2400 AND 800

K-Number: K837139 · 1983-03-04

Decision Date1983-03-04

Product Code

DecisionSubstantially Equivalent

Device Summary

MODELS EUROSUN 2400 AND 800 is the device name listed in this FDA 510(k) record. The listed applicant is Eurosun Scaenda Sol. It received FDA 510(k) clearance on 1983-03-04 under 510(k) number K837139. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODELS EUROSUN 2400 AND 800?

MODELS EUROSUN 2400 AND 800 is a medical device that received FDA 510(k) clearance on 1983-03-04. The listed applicant is Eurosun Scaenda Sol. The 510(k) number is K837139.

When did MODELS EUROSUN 2400 AND 800 receive FDA 510(k) clearance?

MODELS EUROSUN 2400 AND 800 received FDA 510(k) clearance on 1983-03-04, under 510(k) number K837139.

Who is the listed applicant for MODELS EUROSUN 2400 AND 800?

The FDA 510(k) record lists Eurosun Scaenda Sol as the applicant. This does not by itself establish the device manufacturer.

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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.