# K920614: Hemo-Band

- Pathway: 510(k) (Traditional)
- Applicant: Innovations IN Access, Inc.
- Decided: Jul 27, 1992 after 167 days
- Product code: KOC (Accessories, Blood Circuit, Hemodialysis)
- Device class: 2
- Regulation: 21 CFR 876.5820
- 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; 1 cites 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 lists a 510(k) statement for it but has not posted the file, 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/K920614
Methodology: https://510kreport.com/methodology
