# K974205: Knitted Wound Dressing-Standard, WCL and Ribbon

- Pathway: 510(k) (Traditional)
- Applicant: Convatec, A Division of E.R. Squibb & Sons
- Decided: Feb 6, 1998 after 88 days
- Product code: KMF (Bandage, Liquid)
- Device class: 1
- Regulation: 21 CFR 880.5090
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) KERLIX* Super Sponges: named in the summary without a submission number
- (no number) Profore* Wound Contact Layer: named in the summary without a submission number
- (no number) NU Gauze*: named in the summary without a submission number

## Indications for use
Knitted Wound Dressing Standard, WCL and Ribbon can be used in the management of acute and chronic wounds, including diabetic ulcers. The design of Standard makes it suitable for shallow or cavity wounds and Ribbon as a packing strip for cavity wounds, fistulae and sinuses.

Source page: https://510kreport.com/device/K974205
Methodology: https://510kreport.com/methodology