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Pronova Sc360

FDA UDI

Class II (US FDA UDI)

by Pronova Solutions, Llc

Identity

Trade Name
PRONOVA SC360 FDA UDI
Generic Name
Proton therapy system FDA UDI
Device Name
Proton Therapy System FDA UDI
Model / Reference
R1.0 FDA UDI
Description
Proton Therapy System FDA UDI

Identifiers

Primary DI / UDI-DI
00863274000301 FDA UDI
510(k) Number
K162246 FDA UDI
FDA Product Code
LHN FDA UDI
GMDN Term
Proton therapy system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.5050 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

No

FDA UDI

Category: Proton therapy system

Pronova Sc360 by Pronova Solutions, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Proton therapy system.

Cleared under the same submission

K162246 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI aaaedcc4-1118-4636-b684-f1f0cc0ab5e7 34 fields · synced Jun 8, 2026