# K990906: Ferris Polymem Polywic Sterile Cavity Wound Filler

- Pathway: 510(k) (Traditional)
- Applicant: Ferris Mfg. Corp.
- Decided: Apr 29, 1999 after 42 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 no predicate by number.

## Indications for use
Pressure Ulcers (Stage III-IV) Arterial Ulgers Venous Ulcers Diabetic Ulcers

Source page: https://510kreport.com/device/K990906
Methodology: https://510kreport.com/methodology