Qlicksmart BladeFlask UNIVERSAL— 510(k) K213274

Name: FDA 510(k) clearance K213274
Creator: U.S. Food and Drug Administration
Published: 2022-06-22

Substantially Equivalent

Qlicksmart Pty , Ltd.

FDA 510(k) clearance K213274 for Qlicksmart BladeFlask UNIVERSAL, Substantially Equivalent on 2022-06-22. Applicant: Qlicksmart Pty , Ltd.. Device class: 2.

Clearance details

Applicant: Qlicksmart Pty , Ltd.
Product code: Code MMK
Device class: Class 2
Regulation: 21 CFR 880.5570
Advisory panel: General Hospital
Date received: 2021-09-30
Decision date: 2022-06-22
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Brisbane, AU

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.