# K002248: Dinamap Pro 1000 Monitor, Model 1000

- Pathway: 510(k) (Traditional)
- Applicant: Critikon Company, LLC
- Decided: Sep 21, 2000 after 58 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.
31 later devices descend from it; 3 cite it directly.
1 of 32 devices in its family (counting itself) has 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
- K012915: Dinamap Pro 1000 Monitor, Model 1000 (2002), 27 descendants of its own
- K022834: Dinamap Pro 1000 Monitor with Superstat, Model 1000 (2003), 23 descendants of its own
- K073203: Carescape V100 (2007), 20 descendants of its own
- K102426: Carescape Model V100 Vital Signs Monitor (2010), 11 descendants of its own
- K120598: Procare Monitor B40 (2012), 10 descendants of its own

Source page: https://510kreport.com/device/K002248
Methodology: https://510kreport.com/methodology