MiniLoad Syringe
K-Number: K202432 · 2021-02-19
ApplicantOcuject, LLC
Decision Date2021-02-19
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
MiniLoad Syringe is a medical device manufactured by Ocuject, LLC. It received FDA 510(k) clearance on 2021-02-19 under approval number K202432. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the MiniLoad Syringe?
MiniLoad Syringe is a medical device that received FDA 510(k) clearance on 2021-02-19. It is manufactured by Ocuject, LLC. The 510(k) number is K202432.
When was MiniLoad Syringe approved by the FDA?
MiniLoad Syringe received FDA 510(k) clearance on 2021-02-19, under approval number K202432.
What company makes MiniLoad Syringe?
MiniLoad Syringe is manufactured by Ocuject, LLC.
What is the FDA product code for MiniLoad Syringe?
The FDA product code for MiniLoad Syringe is FMF.
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.