# K073261: Var Monitor

- Pathway: 510(k) (Special)
- Applicant: Vortran Medical Technology 1, Inc.
- Decided: May 23, 2008 after 185 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
Longest line of descent: 2 generations back to K944349 (1995). 4 ancestors in all.
1 later device descends from it; 1 cites 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)
- K973975: Respirtechpro, Vortran Medical Technology 1, Inc. (1998) Summary page 1.
- K001430: Respirtech Pro-O2C, Model 2200 and Respirtech Pro, Model 2000, Vortran Medical Technology 1, Inc. (2000) Summary page 1.
- K041473: Var-Plus (Vortran Automatic Resuscitator), Model PCM, Vortran Medical Technology 1, Inc. (2004) Summary page 1.

## Most influential descendants
- K103639: Vortran Airway Pressure Monitor (Vapm)-Adult, Vortran Airway Pressure Monitor (Vapm)- Pediatric (2011), 0 descendants of its own

## Indications for use
The device is to be used by properly trained personnel to deliver emergency, short term, constant flow - pressure cycled ventilatory support.

Source page: https://510kreport.com/device/K073261
Methodology: https://510kreport.com/methodology