Vesco Medical NRFit Tip Syringes
K-Number: K170218 · 2017-02-24
ApplicantVesco Medical, LLC
Decision Date2017-02-24
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
Vesco Medical NRFit Tip Syringes is a medical device manufactured by Vesco Medical, LLC. It received FDA 510(k) clearance on 2017-02-24 under approval number K170218. 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 Vesco Medical NRFit Tip Syringes?
Vesco Medical NRFit Tip Syringes is a medical device that received FDA 510(k) clearance on 2017-02-24. It is manufactured by Vesco Medical, LLC. The 510(k) number is K170218.
When was Vesco Medical NRFit Tip Syringes approved by the FDA?
Vesco Medical NRFit Tip Syringes received FDA 510(k) clearance on 2017-02-24, under approval number K170218.
What company makes Vesco Medical NRFit Tip Syringes?
Vesco Medical NRFit Tip Syringes is manufactured by Vesco Medical, LLC.
What is the FDA product code for Vesco Medical NRFit Tip Syringes?
The FDA product code for Vesco Medical NRFit Tip Syringes is FMF.
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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.