Decision Date1986-02-14
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
TOP SUN is the device name listed in this FDA 510(k) record. The listed applicant is Werner Schott Elektrogerate. It received FDA 510(k) clearance on 1986-02-14 under 510(k) number K854750. 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 TOP SUN?
TOP SUN is a medical device that received FDA 510(k) clearance on 1986-02-14. The listed applicant is Werner Schott Elektrogerate. The 510(k) number is K854750.
When did TOP SUN receive FDA 510(k) clearance?
TOP SUN received FDA 510(k) clearance on 1986-02-14, under 510(k) number K854750.
Who is the listed applicant for TOP SUN?
The FDA 510(k) record lists Werner Schott Elektrogerate as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TOP SUN?
The FDA product code for TOP SUN is FTC.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.