Mini Needle
K-Number: K170768 · 2017-07-10
ApplicantOcuject, LLC
Decision Date2017-07-10
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
Mini Needle is a medical device manufactured by Ocuject, LLC. It received FDA 510(k) clearance on 2017-07-10 under approval number K170768. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Mini Needle?
Mini Needle is a medical device that received FDA 510(k) clearance on 2017-07-10. It is manufactured by Ocuject, LLC. The 510(k) number is K170768.
When was Mini Needle approved by the FDA?
Mini Needle received FDA 510(k) clearance on 2017-07-10, under approval number K170768.
What company makes Mini Needle?
Mini Needle is manufactured by Ocuject, LLC.
What is the FDA product code for Mini Needle?
The FDA product code for Mini Needle is FMI.
Other Devices by Ocuject, LLC
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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.