# K001430: Respirtech Pro-O2C, Model 2200 and Respirtech Pro, Model 2000

- Pathway: 510(k) (Traditional)
- Applicant: Vortran Medical Technology 1, Inc.
- Decided: Jul 5, 2000 after 61 days
- Product code: BTL (Ventilator, Emergency, Powered (Resuscitator))
- Device class: 2
- Regulation: 21 CFR 868.5925
- Recalls of this device: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
5 later devices descend from it; 3 cite it directly.
0 of 6 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
- K041473: Var-Plus (Vortran Automatic Resuscitator), Model PCM (2004), 4 descendants of its own
- K162968: Vortran GO2VENT (2017), 1 descendant of its own
- K073261: Var Monitor (2008), 1 descendant of its own
- K202219: VORTRAN GO2VENT with PEEP Valve (2021), 0 descendants of its own
- K103639: Vortran Airway Pressure Monitor (Vapm)-Adult, Vortran Airway Pressure Monitor (Vapm)- Pediatric (2011), 0 descendants of its own

## Recalls of this device
- Apr 20, 2017 · Class II · Z-2091-2017: Vortran received a customer complaint that the spin-nut-DSS connector was assembled in the reverse direction on the oxygen tubing; making the connector unable to be screwed on due to the wrong thread 
- Apr 20, 2017 · Class II · Z-2092-2017: Vortran received a customer complaint that the spin-nut-DSS connector was assembled in the reverse direction on the oxygen tubing; making the connector unable to be screwed on due to the wrong thread 

Source page: https://510kreport.com/device/K001430
Methodology: https://510kreport.com/methodology