# K991222: Codman Microsensor Ventricular Catheter Kit

- Pathway: 510(k) (Traditional)
- Applicant: Johnson & Johnson Professionals, Inc.
- Decided: Jul 9, 1999 after 88 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
No predicates in its family tree.
12 later devices descend from it; 2 cite it directly.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) CODMAN® MICROSENSOR™ Catheter Kit: named in the summary without a submission number
- (no number) CAMINO NeuroCare™, Inc. Ventrix™ Ventricular Tunneling Pressure Monitoring Kit: named in the summary without a submission number

## Most influential descendants
- K062584: Pressio Icp Monitoring System (2007), 8 descendants of its own
- K103206: Raumedic- Icp-Monitoring System (2011), 7 descendants of its own
- K112017: Raumedic Icp Monitoring System (2011), 6 descendants of its own
- K120252: Raumedic-Icp-Temp-Monitoring-System (2012), 5 descendants of its own
- K130529: Raumedic-Pto-Monitoring-System (2013), 4 descendants of its own

## Indications for use
Use of the CODMAN® MICROSENSOR™ Ventricular Catheter Kit is indicated when direct intracranial pressure (ICP) monitoring is required. The kit is indicated for use in intraventricular pressure monitoring and cerebrospinal fluid (CSF) drainage applications.

Source page: https://510kreport.com/device/K991222
Methodology: https://510kreport.com/methodology