# K920154: BSM-8800A Bedside Monitor

- Pathway: 510(k) (Traditional)
- Applicant: Nihon Kohden America, Inc.
- Decided: Dec 18, 1992 after 340 days
- Product code: DSI (Detector And Alarm, Arrhythmia)
- Device class: 2
- Regulation: 21 CFR 870.1025
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 2 cite it directly.
0 of 4 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
- K971436: Nihon Kohden Tec-7511A/Tec-7521A Cardiolife Portable Defibrillator and Accessories (1997), 1 descendant of its own
- K160667: Anybattery C2 Rechargeable Battery (2017), 0 descendants of its own
- K971355: Nihon Kohden Tec-7531 Cardiolife Portable Defibrillator and Accessories (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K920154
Methodology: https://510kreport.com/methodology