TrapIt
K-Number: K191229 · 2020-01-21
ApplicantImds Operations B.V.
Decision Date2020-01-21
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
TrapIt is a medical device manufactured by Imds Operations B.V.. It received FDA 510(k) clearance on 2020-01-21 under approval number K191229. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the TrapIt?
TrapIt is a medical device that received FDA 510(k) clearance on 2020-01-21. It is manufactured by Imds Operations B.V.. The 510(k) number is K191229.
When was TrapIt approved by the FDA?
TrapIt received FDA 510(k) clearance on 2020-01-21, under approval number K191229.
What company makes TrapIt?
TrapIt is manufactured by Imds Operations B.V..
What is the FDA product code for TrapIt?
The FDA product code for TrapIt is DQY.
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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.