# K900247: CBM-3000/CBM-2000/CBM-7000 Blood Pressure System

- Pathway: 510(k) (Traditional)
- Applicant: Colin Medical Instruments Corp.
- Decided: Jul 17, 1990 after 181 days
- Product code: DXN (System, Measurement, Blood-Pressure, Non-Invasive)
- Device class: 2
- Regulation: 21 CFR 870.1130
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
25 later devices descend from it; 3 cite it directly.
0 of 26 devices 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.

## Most influential descendants
- K060315: Healthstats Bpro Ambulatory Blood Pressure Monitoring System (2006), 19 descendants of its own
- K173028: BPro BT Ambulatory Blood Pressure Monitoring System with BProSoft BT PC Software (2018), 13 descendants of its own
- K190792: BB-613WP (2019), 12 descendants of its own
- K212153: Biobeat Platform, BB-613WP Patch (2022), 5 descendants of its own
- K072593: A-Plus Arterial Pulse Waveform Analysis System and PC Software (2007), 4 descendants of its own

Source page: https://510kreport.com/device/K900247
Methodology: https://510kreport.com/methodology