# K905069: Iodosorb Gel

- Pathway: 510(k) (Traditional)
- Applicant: Perstorp AB C/O Robert Joel Slomoff
- Decided: Jan 31, 1991 after 83 days
- Product code: KOZ (Beads, Hydrophilic, For Wound Exudate Absorption)
- Device class: 1
- Regulation: 21 CFR 878.4018
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 3 cite it directly.
0 of 4 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
- K190730: Iodosorb (2019), 0 descendants of its own
- K122634: Iodofoam Iodophor Foam Dressing (2013), 0 descendants of its own
- K093320: Dryodine Cadexomer-Iodine Gel (2010), 0 descendants of its own

Source page: https://510kreport.com/device/K905069
Methodology: https://510kreport.com/methodology