# K973763: Kendall Curity Iodoform Packing Strip

- Pathway: 510(k) (Traditional)
- Applicant: Kendall Healthcare Products Co. Div.Of Tyco Health
- Decided: Dec 31, 1997 after 90 days
- Product code: EFQ (Gauze/Sponge, Internal)
- Device class: U
- 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) Johnson & Johnson Medical, Inc., NU Gauze® Iodoform Packing Strip: named in the summary without a submission number

## Indications for use
It is indicated for general wound packing.

Source page: https://510kreport.com/device/K973763
Methodology: https://510kreport.com/methodology