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Pegasus

FDA UDI

Class II (US FDA UDI)

by Neuralynx, Inc.

Identity

Trade Name
Pegasus FDA UDI
Generic Name
Electroencephalographic monitoring system FDA UDI
Device Name
Pegasus is the software component of the ATLAS Neurophysiology System that interfaces with the amplifier. It is used to display, store and archive EEG signals and allow user-only annotation and marking. Pegasus does not analyze EEG or automatically detect events. FDA UDI
Model / Reference
2.3.1 FDA UDI
Description
Pegasus is the software component of the ATLAS Neurophysiology System that interfaces with the amplifier. It is used to display, store and archive EEG signals and allow user-only annotation and marking. Pegasus does not analyze EEG or automatically detect events. FDA UDI

Identifiers

Catalog Number
36-0301-0001 FDA UDI
Primary DI / UDI-DI
00867718000278 FDA UDI
510(k) Number
K110967 FDA UDI
FDA Product Code
OMC FDA UDI
GMDN Term
Electroencephalographic monitoring system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electroencephalographic monitoring system

Pegasus by Neuralynx, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electroencephalographic monitoring system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Neuralynx, Inc.

Sources (1)

  • FDA UDI 09e4bf7a-64d5-4fe4-8586-9cff95330d1a 36 fields · synced May 31, 2026