# K973717: Combiderm Acd

- Pathway: 510(k) (Traditional)
- Applicant: Convatec, A Bristol-Myers Squibb Co.
- Decided: Dec 17, 1997 after 79 days
- Product code: FRO (Dressing, Wound, Drug)
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K962590 (1996). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K962590: Signaldress, Convatec, A Division of E.R. Squibb & Sons (1996) Summary page 1.

## Indications for use
CombiDERM ACD is a moisture retentive dressing and is indicated for use on exuding chronic dermal ulcers including full-thickness wounds, such as pressure ulcers, leg ulcers and diabetic ulcers, and on acute wounds such as abrasions, lacerations, biopsies, and open and closed surgical wounds. The dressing provides a moist wound environment that is supportive of the healing process.

Source page: https://510kreport.com/device/K973717
Methodology: https://510kreport.com/methodology