# K031131: Klinidrape Surgical Drapes

- Pathway: 510(k) (Traditional)
- Applicant: Molnlycke Health Care
- Decided: Jun 10, 2003 after 62 days
- Product code: KKX (Drape, Surgical, Antimicrobial)
- Device class: 2
- Regulation: 21 CFR 878.4370
- 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 K000906 (2000). 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)
- K000906: Klinidrape Surgical Drapes, Molnlycke Health Care, Inc. (2000) Summary page 1.

## Indications for use
The Klinidrape@Surgical Drapes are devices intended to be used as a protective patient covering, such as to isolate a site of surgical incision from microbial and other contamination.

Source page: https://510kreport.com/device/K031131
Methodology: https://510kreport.com/methodology