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BrainSpec Core™ Software

FDA UDI

Class II (US FDA UDI)

by Brainspec, Inc

Identity

Trade Name
BrainSpec Core™ Software FDA UDI
Generic Name
Radiological PACS software FDA UDI
Device Name
BrainSpec Core™ Software is a web-based software platform that allows for the interpretation of magnetic spectroscopy data to display relative levels of brain metabolites. FDA UDI
Model / Reference
BrainSpec Core™ Software FDA UDI
Description
BrainSpec Core™ Software is a web-based software platform that allows for the interpretation of magnetic spectroscopy data to display relative levels of brain metabolites. FDA UDI

Identifiers

Primary DI / UDI-DI
00860013965204 FDA UDI
510(k) Number
K230856 FDA UDI
FDA Product Code
LLZ FDA UDI
LNI FDA UDI
GMDN Term
Radiological PACS software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.2050 FDA UDI
892.1000 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: Radiological PACS software

BrainSpec Core™ Software by Brainspec, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiological PACS software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Brainspec, Inc

Sources (1)

  • FDA UDI e13017d6-e664-477a-b56b-9ea2ad212eb7 34 fields · synced May 30, 2026