FEELject LDV (Low dead volume) syringe
K-Number: K213010 · 2023-05-31
ApplicantFeeltech Co., Ltd.
Decision Date2023-05-31
Product CodeQNQ
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
FEELject LDV (Low dead volume) syringe is a medical device manufactured by Feeltech Co., Ltd.. It received FDA 510(k) clearance on 2023-05-31 under approval number K213010. The device is classified under product code QNQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the FEELject LDV (Low dead volume) syringe?
FEELject LDV (Low dead volume) syringe is a medical device that received FDA 510(k) clearance on 2023-05-31. It is manufactured by Feeltech Co., Ltd.. The 510(k) number is K213010.
When was FEELject LDV (Low dead volume) syringe approved by the FDA?
FEELject LDV (Low dead volume) syringe received FDA 510(k) clearance on 2023-05-31, under approval number K213010.
What company makes FEELject LDV (Low dead volume) syringe?
FEELject LDV (Low dead volume) syringe is manufactured by Feeltech Co., Ltd..
What is the FDA product code for FEELject LDV (Low dead volume) syringe?
The FDA product code for FEELject LDV (Low dead volume) syringe is QNQ.
Other Devices by Feeltech Co., Ltd.
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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.