# K890876: BP-8800 Blood Pressure Monitor

- Pathway: 510(k) (Traditional)
- Applicant: Colin Medical Instruments Corp.
- Decided: Jun 22, 1989 after 121 days
- Product code: DRT (Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm))
- Device class: 2
- Regulation: 21 CFR 870.2300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
51 later devices descend from it; 2 cite it directly.
0 of 52 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
- K022537: Press-Mate PM-2100 Vital Sign Monitor (2002), 50 descendants of its own
- K071645: Model HBP T-105 Series, Model T-105 and T-105S (2007), 28 descendants of its own
- K082812: Omron Model HBP-2070 Vital Signs Monitor (2008), 27 descendants of its own
- K112478: Visi Mobile Monitoring System (2012), 24 descendants of its own
- K122036: Visi Mobile Monitoring System (2012), 20 descendants of its own

Source page: https://510kreport.com/device/K890876
Methodology: https://510kreport.com/methodology