# K905768: Pleur-Evac Chest Drainage Systems

- Pathway: 510(k) (Traditional)
- Applicant: Deknatel, Inc.
- Decided: Feb 11, 1991 after 46 days
- Product code: KDQ (Bottle, Collection, Vacuum)
- Device class: 2
- Regulation: 21 CFR 880.6740
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
9 later devices descend from it; 3 cite it directly.
0 of 10 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
- K963850: Pleur-Evac Sahara Plus Model S-1150 Continuous Reinfusion Autotransfusion System (1997), 5 descendants of its own
- K962856: Pleur-Evac Sahara Adult/Pediatric Chest Drainage System Model S-1100, S-1200, 2-2100, and S-2200 with Model S-100 Autotr (1996), 5 descendants of its own
- K031554: S-1150 Pleur-Evac Sahara Plus Continuous Reinfusion Autotransfusion System (2003), 4 descendants of its own
- K120953: Pleur-Evac Sahara Plus Continous Reinfusion Autotransfusion System (2012), 3 descendants of its own
- K130043: Pleur-Evac Sahara Plus Continuous Reinfusion Autotransfusion System (2013), 2 descendants of its own

Source page: https://510kreport.com/device/K905768
Methodology: https://510kreport.com/methodology