# K030803: Parapac 200D Transport, Model V200D

- Pathway: 510(k) (Traditional)
- Applicant: Pneupac, Ltd.
- Decided: Sep 29, 2003 after 200 days
- Product code: BTL (Ventilator, Emergency, Powered (Resuscitator))
- Device class: 2
- Regulation: 21 CFR 868.5925
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
10 later devices descend from it; 1 cites it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) babyPAC: named in the summary without a submission number
- (no number) paraPAC ‘medic’: named in the summary without a submission number

## Most influential descendants
- K043085: Modification to: Pneuton Ventilator (2004), 9 descendants of its own
- K080692: Macs Cpap System (2008), 7 descendants of its own
- K092085: Ispira Resuscitation Unit (2009), 4 descendants of its own
- K102649: Neopop Infant Resuscitator with Flow Meter (2011), 2 descendants of its own
- K110119: Pressure Manometer (2011), 1 descendant of its own

## Indications for use
The paraPAC 200D ‘Transport’ ventilator is a portable, gas powered. time-cycled ventilator that is designed for ventilation during transportation and emergency ventilation of patients who have respiratory distress or insufficiency.

Source page: https://510kreport.com/device/K030803
Methodology: https://510kreport.com/methodology