# K936108: Masterscreen Body

- Pathway: 510(k) (Traditional)
- Applicant: Erich Jaeger GmbH & Co. KG
- Decided: Feb 3, 1995 after 403 days
- Product code: JEH (Plethysmograph, Volume)
- Device class: 2
- Regulation: 21 CFR 868.1760
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
10 later devices descend from it; 1 cites it directly.
1 of 11 devices in its family (counting itself) has 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
- K122699: Sentrysuite Product Line (2012), 9 descendants of its own
- K133925: Vyntus/ Sentrysuite Product Line (2014), 8 descendants of its own
- K150810: Vyntus / SentrySuite Product Line (2015), 5 descendants of its own
- K242809: Ascent Cardiorespiratory Diagnostic Software (2024), 1 descendant of its own
- K181524: Vyntus ONE with CART, Vyntus ONE PFT only with CART, Vyntus ONE with adjustable CART, Vyntus ONE PFT only with adjustable CART (2018), 1 descendant of its own

Source page: https://510kreport.com/device/K936108
Methodology: https://510kreport.com/methodology