# K973509: Kendall Curasorb ZN + MG Alginate Wound Dressing

- Pathway: 510(k) (Traditional)
- Applicant: Kendall Healthcare Products Co. Div.Of Tyco Health
- Decided: Dec 4, 1997 after 79 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) Kendall CURASORB® Calcium Alginate Dressing: named in the summary without a submission number
- (no number) Kendall CURASORB® Zn Alginate Wound Dressing: named in the summary without a submission number

## Indications for use
The proposed device is for use in the management of wounds which present moderate to heavy wound exudate such as dermal ulcers (i.e., venous stasis, pressure, arterial, diabetic); traumatic wounds (i.e., lacerations, punctures, abrasions or incisions); donor sites; and second-degree burns.

Source page: https://510kreport.com/device/K973509
Methodology: https://510kreport.com/methodology