# K940013: Body Position Indicator, Model BPI1

- Pathway: 510(k) (Traditional)
- Applicant: Pro-Tech, Inc.
- Decided: May 4, 1995 after 485 days
- Product code: MNR (Ventilatory Effort Recorder)
- Device class: 2
- Regulation: 21 CFR 868.2375
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
102 later devices descend from it; 2 cite it directly.
0 of 103 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K020607: Sleepflo, Model 101501 (2002), 99 descendants of its own
- K030379: Aplab, Model 801D0030 (2003), 98 descendants of its own
- K041904: Compass F10 System (2004), 54 descendants of its own
- K073682: Embletta Gold (2008), 41 descendants of its own
- K041724: Compass M10 System (2004), 41 descendants of its own

Source page: https://510kreport.com/device/K940013
Methodology: https://510kreport.com/methodology