ToFscan
K-Number: K172690 · 2018-05-31
ApplicantIdmed
Decision Date2018-05-31
Product CodeKOI
Advisory CommitteeAN
DecisionSubstantially Equivalent
Device Summary
ToFscan is a medical device manufactured by Idmed. It received FDA 510(k) clearance on 2018-05-31 under approval number K172690. The device is classified under product code KOI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the ToFscan?
ToFscan is a medical device that received FDA 510(k) clearance on 2018-05-31. It is manufactured by Idmed. The 510(k) number is K172690.
When was ToFscan approved by the FDA?
ToFscan received FDA 510(k) clearance on 2018-05-31, under approval number K172690.
What company makes ToFscan?
ToFscan is manufactured by Idmed.
What is the FDA product code for ToFscan?
The FDA product code for ToFscan is KOI.
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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.