# K992743: Collins CPL

- Pathway: 510(k) (Special)
- Applicant: Collins Medical, Inc.
- Decided: Sep 13, 1999 after 28 days
- Product code: BZG (Spirometer, Diagnostic)
- Device class: 2
- Regulation: 21 CFR 868.1840
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
7 later devices descend from it; 3 cite it directly.
0 of 8 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
- K052328: Zan Lung-Function Lab (2005), 4 descendants of its own
- K133051: Pulmone Minibox PFT TM (2014), 3 descendants of its own
- K141793: Pulmone Miniboxpft 2.0 (2015), 2 descendants of its own
- K161295: MiniBox + (2016), 1 descendant of its own
- K030464: Gem, Model 004110 (2003), 1 descendant of its own

## Indications for use
The Collins CPL Pulmonary Function Test System is intended as a configuraple non-invasive pulmonary function testing (PFT), and exercise/nutritional/metabolic testing system. Complete plethysmography capabilities are an optional module. These tests are suitable for both pediatric and adult patient testing.

Source page: https://510kreport.com/device/K992743
Methodology: https://510kreport.com/methodology