FDA 510(k)

Qlicksmart BladeFlask UNIVERSAL

K-Number: K213274 · 2022-06-22

Decision Date2022-06-22

Product CodeMMK

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

Qlicksmart BladeFlask UNIVERSAL is a medical device manufactured by Qlicksmart Pty , Ltd.. It received FDA 510(k) clearance on 2022-06-22 under approval number K213274. The device is classified under product code MMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Qlicksmart BladeFlask UNIVERSAL?

Qlicksmart BladeFlask UNIVERSAL is a medical device that received FDA 510(k) clearance on 2022-06-22. It is manufactured by Qlicksmart Pty , Ltd.. The 510(k) number is K213274.

When was Qlicksmart BladeFlask UNIVERSAL approved by the FDA?

Qlicksmart BladeFlask UNIVERSAL received FDA 510(k) clearance on 2022-06-22, under approval number K213274.

What company makes Qlicksmart BladeFlask UNIVERSAL?

Qlicksmart BladeFlask UNIVERSAL is manufactured by Qlicksmart Pty , Ltd..

What is the FDA product code for Qlicksmart BladeFlask UNIVERSAL?

The FDA product code for Qlicksmart BladeFlask UNIVERSAL is MMK.

Related Devices (Code: MMK)

K153274Med-Tainer Single Deposit ContainerSnyder Industries, Inc. K153363Red2Green Reusable Sharps ContainerTriumvirate Environmental, Inc. K161180Oak Ridge Products Sharps ContainersOak Ridge Products, LLC K152340NAR Sharps Shuttle; NAR Sharps Shuttle Pack of sixNorth American Rescue, LLC K170513MAUSER PG II Sharps ContainerMauzer USA, LLC K172719HealthBeacon HB2 Sharps BinHealthbeacon, Ltd.

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.