# K051599: Neurorecovery, Inc. (Nri) Comprehensive Intracranial Pressure Evaluation and Relief (Ciper) Kit

- Pathway: 510(k) (Traditional)
- Applicant: Neurorecovery, Inc.
- Decided: Jul 19, 2005 after 33 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: 1 generation back to K822864 (1982). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K822864: Intracranial Pressure Monitoring Device, Medex, Inc. (1982) Summary page 1.
- K020780: Transtar Intracranial Pressure Transducer, Model MX950ICP, Medex, Inc. (2002) Summary page 1.

## Indications for use
The Neurorecovery™, Inc., Neurorecovery Comprehensive Intracranial Pressure Evaluation and Relief Kit (NRI CIPER™ Kit) is intended for single patient use for the measurement of intracranial pressures (ICP) and drainage of Cerebral Spinal Fluid (CSF). It is intended for short term management of patients with increased intracranial pressure.

Source page: https://510kreport.com/device/K051599
Methodology: https://510kreport.com/methodology