# K943393: Civco Probe Boot/Cord Cover

- Pathway: 510(k) (Traditional)
- Applicant: CIVCO Medical Instruments Co., Inc.
- Decided: Feb 2, 1995 after 203 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.
2 later devices descend from it; 2 cite it directly.
0 of 3 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
- K974301: CLK Int'l. Sanitary Latex Probe Cover, CLK Ultrasound Probe Cover (1998), 0 descendants of its own
- K970891: Drape, Surgical-Latex (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K943393
Methodology: https://510kreport.com/methodology