# K023536: Nuamps

- Pathway: 510(k) (Abbreviated)
- Applicant: Neuroscan
- Decided: Jan 15, 2003 after 86 days
- Product code: OLT (Non-Normalizing Quantitative Electroencephalograph Software)
- Device class: 2
- Regulation: 21 CFR 882.1400
- 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 K001564 (2000). 1 ancestor in all.
20 later devices descend from it; 1 cites it directly.
0 of 22 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K001564: Scan LT40 (40 Channels), Neuro Scan Labs (2000) Summary page 1.

## Most influential descendants
- K060803: G.Usbamp (2006), 19 descendants of its own
- K090957: Blackrock Neuroport Biopotential Signal Processing System (2009), 13 descendants of its own
- K103140: Nicolet Wireless Eeg (2011), 7 descendants of its own
- K123255: g.HIamp (2012), 4 descendants of its own
- K122196: Cervello Bio-Potential Signal Acquistion System Product Family (2013), 3 descendants of its own

## Indications for use
The Neuroscan Nuamps® system is intended for the measuring recording and analysis of the electrical activity of a paticnt’s brain and/or through the attachment of multiple electrodes at various locations to aid in monitoring and diagnosis as routinely found in clinical settings for EEG. The system is intended for the EEG and long/middle-latency EP registration in the research environment

Source page: https://510kreport.com/device/K023536
Methodology: https://510kreport.com/methodology