# K213274: Qlicksmart BladeFlask UNIVERSAL

- Pathway: 510(k) (Abbreviated)
- Applicant: Qlicksmart Pty, Ltd.
- Decided: Jun 22, 2022 after 265 days
- Product code: MMK (Container, Sharps)
- Device class: 2
- Regulation: 21 CFR 880.5570
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K983367 (1998). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K983367: Qlicksmart, Handren Assoc. (1998) Summary page 5.

## Indications for use
The Qlicksmart BladeFlask PLUS is a single-use sharps container with a scalpel blade removal function intended to permit the safe removal of scalpel blades from most currently available scalpel handles and contain the blade immediately upon removal to eliminate the need for further handling prior to be disposed as medical waste while allowing the user to monitor its use to see when it is becoming full and will need changing. Scalpel handles compatible with the Qlicksmart BladeFlask PLUS include: Swann Morton sizes 3, 4, 5, 6, 7, 8, and 9 Lawton size 4 Martin sizes 3, 4, and 7 Aesculap sizes 3, 4, 6, and 7 Sayco sizes 3, 4, and 5 Smic sizes 3 and 4 Nopa sizes 3 and 4 AB Stainless size 4 Lance sizes 3 and 4 Pro-Med sizes 3 and 4 Paragon sizes 3 and 4 Rocket size 5 Conqueror size 3 Feather sizes 3, 4, and 7 LRI sizes 3 and 4 Generic handle size 4 L-dent Medesy size 5 Jakobi size 4 CS size 5 Helmut Zepf Scalpel handles known to be incompatible with the Qlicksmart BladeFlask PLUS include: Beaver type handles Disposable handles

Source page: https://510kreport.com/device/K213274
Methodology: https://510kreport.com/methodology