NeedleSmart Professional (NS Pro)
K-Number: K202073 · 2021-03-25
ApplicantNeedlesmart Limited
Decision Date2021-03-25
Product CodeMTV
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
NeedleSmart Professional (NS Pro) is a medical device manufactured by Needlesmart Limited. It received FDA 510(k) clearance on 2021-03-25 under approval number K202073. The device is classified under product code MTV. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the NeedleSmart Professional (NS Pro)?
NeedleSmart Professional (NS Pro) is a medical device that received FDA 510(k) clearance on 2021-03-25. It is manufactured by Needlesmart Limited. The 510(k) number is K202073.
When was NeedleSmart Professional (NS Pro) approved by the FDA?
NeedleSmart Professional (NS Pro) received FDA 510(k) clearance on 2021-03-25, under approval number K202073.
What company makes NeedleSmart Professional (NS Pro)?
NeedleSmart Professional (NS Pro) is manufactured by Needlesmart Limited.
What is the FDA product code for NeedleSmart Professional (NS Pro)?
The FDA product code for NeedleSmart Professional (NS Pro) is MTV.
Related Devices (Code: MTV)
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.