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Sr-130-C

FDA UDI

Class II (US FDA UDI)

by Source-Ray, Inc.

Identity

Trade Name
SR-130-C FDA UDI
Generic Name
Diagnostic x-ray system generator, mobile FDA UDI
Device Name
X-Ray Control, 100kVp / 30 mA FDA UDI
Model / Reference
SR-130-C FDA UDI
Description
X-Ray Control, 100kVp / 30 mA FDA UDI

Identifiers

Catalog Number
910002 FDA UDI
Primary DI / UDI-DI
00868162000258 FDA UDI
510(k) Number
K030494 FDA UDI
FDA Product Code
IZL FDA UDI
GMDN Term
Diagnostic x-ray system generator, mobile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1720 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: Diagnostic x-ray system generator, mobile

Sr-130-C by Source-Ray, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Diagnostic x-ray system generator, mobile.

Cleared under the same submission

K030494 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Source-Ray, Inc.

Sources (1)

  • FDA UDI b0cbbeb5-ae6f-41b0-847a-f1d016b48d38 36 fields · synced May 30, 2026