# K013390: Quickclot

- Pathway: 510(k) (Traditional)
- Applicant: On Site Gas Systems, Inc.
- Decided: May 23, 2002 after 220 days
- Product code: QSY (Hemostatic Wound Dressing Without Thrombin Or Other Biologics)
- Device class: U
- 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 K002550 (2000). 1 ancestor in all.
64 later devices descend from it; 8 cite it directly.
0 of 66 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K002550: RDH Bandage, Marine Polymer Technologies, Inc. (2000) Summary page 6.

## Most influential descendants
- K051955: Quickclot Acs - Accelerated Clotting Sponge (2005), 42 descendants of its own
- K061767: Quikclot 1ST Response & Quikclot Acs+ (2006), 39 descendants of its own
- K070010: Quikclot Sport and Quikclot Sport Silver (2007), 38 descendants of its own
- K072474: Quikclot EX (2007), 36 descendants of its own
- K061079: Medtrade Products Celox Topical Hemostatic Granules, Medtrade Products Celox 762 Hemostatic Granules (2006), 27 descendants of its own

## Indications for use
QuikClot is intended for emergency use only as an external temporary traumatic wound treatment to achieve hemostasis for moderate to severe wounds.

Source page: https://510kreport.com/device/K013390
Methodology: https://510kreport.com/methodology