# K042728: Camino Slim-Line Intracranial Monitoring System

- Pathway: 510(k) (Traditional)
- Applicant: Novus Monitoring, Ltd.
- Decided: Oct 22, 2004 after 21 days
- Product code: GWM (Device, Monitoring, Intracranial Pressure)
- Device class: 2
- Regulation: 21 CFR 882.1620
- 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 K875179 (1988). 9 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K013930: Neurosensor, Novus Monitoring, Ltd. (2002) Summary page 1.
- K914479: Microsensor Intracranial Pressure Transducer, Codman & Shurtleff, Inc. (1994) Summary page 1.
- K853864: Intracranial Pressure Monitoring Kit 070, Camino Laboratories, Inc. (1986) Summary page 1.

## Most influential descendants
- K172209: Aura Icp Monitoring System (2018), 0 descendants of its own

## Indications for use
The Camino Slim-LineTM Intracranial Monitoring System has been designed for use by a qualified neurosurgeon in the direct monitoring of intracranial pressure in both sub-dural and intraparenchymal applications.

Source page: https://510kreport.com/device/K042728
Methodology: https://510kreport.com/methodology