Sr-130-C
Sr-130-C (910002) is a Class II device made by Source-Ray, Inc., cleared under FDA 510(k) K030494 on 20 May 2003 and listed in FDA GUDID since 9 Sep 2016 (UDI-DI 00868162000258), active as of 21 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00868162000258 | Date9 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK030494 | Date20 May 2003 | StatusActive |
Official records
- AccessGUDID record 00868162000258
- FDA 510(k) database K030494
Across registries
- FDA 510(k) K030494 decided 20 May 2003 Active
- FDA GUDID UDI-DI 00868162000258 listed 9 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K030494
- Listed FDA GUDID 00868162000258
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Generic name
- Diagnostic x-ray system generator, mobile
- Model / Ref / Catalog
- SR-130-C, 910002
- Primary DI / UDI-DI
- 00868162000258
- 510(k) Number
- FDA product code
- IZL
- GMDN term
- Diagnostic x-ray system generator, mobile
- Device class
- Class II
- Regulation number
- 892.1720
- GUDID distribution status
- In Commercial Distribution
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