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Option, Pediatric Scanning Platform

FDA UDI

Class II (US FDA UDI)

by Neurologica Corporation

Identity

Trade Name
OPTION, PEDIATRIC SCANNING PLATFORM FDA UDI
Generic Name
Basic diagnostic x-ray system table, non-powered FDA UDI
Model / Reference
0-00079-001 FDA UDI

Identifiers

Primary DI / UDI-DI
10815411020069 FDA UDI
510(k) Number
K172539 FDA UDI
FDA Product Code
JAK FDA UDI
GMDN Term
Basic diagnostic x-ray system table, non-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1750 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Basic diagnostic x-ray system table, non-powered

Option, Pediatric Scanning Platform by Neurologica Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic diagnostic x-ray system table, non-powered.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 794a8b81-afa2-45a7-bd43-bbaf1120b339 33 fields · synced May 30, 2026