# K103639: Vortran Airway Pressure Monitor (Vapm)-Adult, Vortran Airway Pressure Monitor (Vapm)- Pediatric

- Pathway: 510(k) (Traditional)
- Applicant: Vortran Medical Technology 1, Inc.
- Decided: Sep 15, 2011 after 276 days
- Product code: CAP (Monitor, Airway Pressure (Includes Gauge And/Or Alarm))
- Device class: 2
- Regulation: 21 CFR 868.2600
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K944349 (1995). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K073261: Var Monitor, Vortran Medical Technology 1, Inc. (2008) 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.

## Indications for use
The VORTRAN Airway Pressure Monitor (VAPM) is to be used by properly trained personnel to monitor the delivery of emergency, shodt term, ventilatory suppodt to adult (using VAPM-3900 Adult Model) and/or pediatric (using VAPM-3800 Pediatric Model).

Source page: https://510kreport.com/device/K103639
Methodology: https://510kreport.com/methodology