# K021520: Emt-Cpap

- Pathway: 510(k) (Traditional)
- Applicant: Emergency Medical Techology
- Decided: Jul 15, 2002 after 66 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.
8 later devices descend from it; 2 cite it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- 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
- K093862: Carevent Handheld Cpap System (2010), 1 descendant of its own

## Indications for use
To provide CPAP to spontaneously breathing patients in the hospital and pre-hospital (EMS) environments.

Source page: https://510kreport.com/device/K021520
Methodology: https://510kreport.com/methodology