# K060756: Medlog, Model 1-0-10

- Pathway: 510(k) (Traditional)
- Applicant: Bmc Gesellschaft Fur Medizintechnik Mbh
- Decided: Oct 30, 2006 after 223 days
- Product code: MWI (Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms))
- 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
Longest line of descent: 4 generations back to K000635 (2000). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K032142: Datacaptor, Capsule Technologie (2003) Summary page 1.

## Indications for use
The MEDLOG System is indicated for the use in data collection and clinical information management. MEDLOG is connected with independent bedside or clinical devices either directly of through networks. The MEDLOG is not intended for monitoring purposes, nor is the software intended to control any of the clinical devices, which is connected to.

Source page: https://510kreport.com/device/K060756
Methodology: https://510kreport.com/methodology