# K942014: Sterile Water Wet Dressing

- Pathway: 510(k) (Traditional)
- Applicant: Trinity Laboratories, Inc.
- Decided: May 27, 1994 after 31 days
- Product code: MGF
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
11 later devices descend from it; 1 cites it directly.
0 of 12 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
- K033398: Laryngeal Augmentation Implant (2003), 10 descendants of its own
- K060815: Juliesse Injectable Laryngeal Augmentation Implant (2006), 6 descendants of its own
- K070090: Radiesse Laryngeal Implant (2007), 5 descendants of its own
- K071663: VF Gel Plus (2008), 4 descendants of its own
- K080956: Modification to VF Gel Plus (2008), 3 descendants of its own

Source page: https://510kreport.com/device/K942014
Methodology: https://510kreport.com/methodology