# K002550: RDH Bandage

- Pathway: 510(k) (Traditional)
- Applicant: Marine Polymer Technologies, Inc.
- Decided: Dec 20, 2000 after 125 days
- Product code: KMF (Bandage, Liquid)
- Device class: 1
- Regulation: 21 CFR 880.5090
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
99 later devices descend from it; 4 cite it directly.
0 of 100 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K023298: Hemcon Bandage (2002), 74 descendants of its own
- K013390: Quickclot (2002), 64 descendants of its own
- K030946: Hemcon Bandage Otc; Hemcon Cath/Aid (2003), 56 descendants of its own
- K043050: Hemcon Bandage and Hemcon Bandage Otc (2005), 55 descendants of its own
- K051955: Quickclot Acs - Accelerated Clotting Sponge (2005), 42 descendants of its own

Source page: https://510kreport.com/device/K002550
Methodology: https://510kreport.com/methodology