Identity
- Trade Name
- OPTION, NL4X00 WS-240V FDA UDI
- Generic Name
- CT system workstation FDA UDI
- Model / Reference
- 0-00132-003 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10815411020816 FDA UDI
- FDA Product Code
- JAK FDA UDI
- GMDN Term
- CT system workstation 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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: CT system workstation
Option, Nl4x00 Ws-240v by Neurologica Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as CT system workstation.
- HOLOSCOPE — Real View Imaging , Ltd. · Class II
- OPTION, WS CART NL4000 — Neurologica Corporation · Class II
- OPTION, NL4X00 WS-240V-S — Neurologica Corporation · Class II
- OPTION, NL4X00 WS-120V-S — Neurologica Corporation · Class II
- Scanner Drive System — Neurologica Corporation · Class II
- Mobile ENT Computer Cart, Assembly — Neurologica Corporation · Class II
Cleared under the same submission
K170238 also covers:
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Neurologica Corporation
Sources (1)
- FDA UDI 6c42c38c-7893-415e-a0e9-6a87d4134815 33 fields · synced May 30, 2026