# K983582: Cardiobeeper CB250

- Pathway: 510(k) (Traditional)
- Applicant: Merdian Medical Technologies, Ltd.
- Decided: Nov 13, 1998 after 31 days
- Product code: DXH (Transmitters And Receivers, Electrocardiograph, Telephone)
- Device class: 2
- Regulation: 21 CFR 870.2920
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K813101 (1981). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K883843: Cardiobeeper II, Survival Technology, Inc. (1988) Summary page 2.
- K965101: Cardiobeeper CB-12L, Meridian Medical Technologies, Inc. (1997) Summary page 2.

## Indications for use
The CardioBeeper CB250 is indicated for use by the patient in transmitting ECG information from a remote location to a receiving center.

Source page: https://510kreport.com/device/K983582
Methodology: https://510kreport.com/methodology