# K003939: Venture Home Fill II, Model Ioh 200

- Pathway: 510(k) (Traditional)
- Applicant: Invacare Corp.
- Decided: Mar 21, 2001 after 90 days
- Product code: CAW (Generator, Oxygen, Portable)
- Device class: 2
- Regulation: 21 CFR 868.5440
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
11 later devices descend from it; 6 cite it directly.
0 of 12 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
- K020330: Deployable Oxygen Concentration System (Docs) (2002), 5 descendants of its own
- K040738: Mobile Oxygen Storage Tank (Most) (2004), 2 descendants of its own
- K091191: Gas Transfill (2009), 1 descendant of its own
- K061414: Expeditionary Delployable Oxygen Concentration System (Edocs), Models 120B and 30;Mobile Oxygen Storage Tank (Most), Mod (2007), 1 descendant of its own
- K050430: Merits Health Products Oxygen Concentrator (2005), 1 descendant of its own

## Recalls of this device
- Jan 11, 2011 · Not classified · Z-1423-2011: Invacare Corporation decided to recall the products because risk analysis reveals that inadequate clearance between a motor ground clip and the motor windings may result in an increased risk for shock

Source page: https://510kreport.com/device/K003939
Methodology: https://510kreport.com/methodology