# K945835: Argidene (TM) Gel

- Pathway: 510(k) (Traditional)
- Applicant: Telios Pharmaceuticals, Inc.
- Decided: Feb 13, 1995 after 76 days
- Product code: MGQ (Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic)
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
64 later devices descend from it; 2 cite it directly.
1 of 65 devices in its family (counting itself) has 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
- K984413: Bionect Hydrogel (1999), 60 descendants of its own
- K020325: L.a.M. Ipm Wound Gel (2002), 59 descendants of its own
- K090725: Oculus Microcyn Wound Gel (2009), 56 descendants of its own
- K100918: Vashe Wound Therapy System Model: 9000-0014 (2010), 31 descendants of its own
- K123072: Vashe Wound Therapy Solution (2013), 25 descendants of its own

Source page: https://510kreport.com/device/K945835
Methodology: https://510kreport.com/methodology