# K873806: JDM SP2 Sensor

- Pathway: 510(k) (Traditional)
- Applicant: Jd Monitoring C/O Mackler, Cooper and Gibbs
- Decided: Dec 8, 1987 after 81 days
- Product code: KMI (Monitor, Bed Patient)
- Device class: 1
- Regulation: 21 CFR 880.2400
- Recalls of this device: 4 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

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

## Recalls of this device
- Mar 26, 2010 · Not classified · Z-1945-2010: Product might not indicate low battery alarms or exit alarms when powered by a DC power supply.
- Mar 26, 2010 · Not classified · Z-1944-2010: Product might not indicate low battery alarms or exit alarms when powered by a DC power supply.
- Mar 26, 2010 · Not classified · Z-1947-2010: Product might not indicate low battery alarms or exit alarms when powered by a DC power supply.
- Mar 26, 2010 · Not classified · Z-1946-2010: Product might not indicate low battery alarms or exit alarms when powered by a DC power supply.

Source page: https://510kreport.com/device/K873806
Methodology: https://510kreport.com/methodology