NeedleSmart Professional (NS Pro)— 510(k) K202073

Name: FDA 510(k) clearance K202073
Creator: U.S. Food and Drug Administration
Published: 2021-03-25

Substantially Equivalent

Needlesmart Limited

FDA 510(k) clearance K202073 for NeedleSmart Professional (NS Pro), Substantially Equivalent on 2021-03-25. Applicant: Needlesmart Limited. Device class: 2.

Clearance details

Applicant: Needlesmart Limited
Product code: Code MTV
Device class: Class 2
Regulation: 21 CFR 880.6210
Advisory panel: General Hospital
Date received: 2020-07-27
Decision date: 2021-03-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Knowsley, Prescot, GB

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