# K941176: Alginate Fiber

- Pathway: 510(k) (Traditional)
- Applicant: Adri/Technam
- Decided: Jul 28, 1994 after 136 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.
15 later devices descend from it; 2 cite it directly.
0 of 16 devices in its family (counting itself) have a Class I recall.

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

## Most influential descendants
- K040208: Neptune Pad, Neptune Disc, Neptune Comfort-Band, Comfort-Band (2004), 14 descendants of its own
- K092503: Radar Vascular Compression Devices (2009), 9 descendants of its own
- K111837: Radial Artery Compression Tourniquet (2011), 4 descendants of its own
- K142122: Radar Vascular Compression Device (2014), 3 descendants of its own
- K142359: Vasc Band hemostat (2014), 3 descendants of its own

Source page: https://510kreport.com/device/K941176
Methodology: https://510kreport.com/methodology