# K000442: Acti-Gard Antimicrobial Film, Models D6635, D6640, D6648, D6650,D6651, D66XX

- Pathway: 510(k) (Traditional)
- Applicant: Medical Concepts Development, Inc.
- Decided: Apr 24, 2001 after 439 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
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K052870: Integuseal Microbial Sealant, Model IS 100 and 1S200 (2006), 0 descendants of its own

Source page: https://510kreport.com/device/K000442
Methodology: https://510kreport.com/methodology