QuickLink™, SourceLink™ 70301QC20
QuickLink, SourceLink 70301QC20 is a brachytherapy source spacer (FDA Class II; FDA product code KXK, Source, brachytherapy, radionuclide) made by Bard Brachytherapy, Inc, cleared under FDA 510(k) K023210 on 28 Mar 2003 and listed in FDA GUDID since 5 Oct 2015 (UDI-DI 10801741078078), active as of 23 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 | Number10801741078078 | Date5 Oct 2015 | StatusListed |
| United States | FDA 510(k)SESE | NumberK023210 | Date28 Mar 2003 | StatusActive |
Official records
- AccessGUDID record 10801741078078
- FDA 510(k) database K023210
Across registries
- FDA 510(k) K023210 decided 28 Mar 2003 Active
- FDA GUDID UDI-DI 10801741078078 listed 5 Oct 2015 Listed
Timeline
- Cleared FDA 510(k) K023210
- Listed FDA GUDID 10801741078078
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- QuickLink™, SourceLink™
- Generic name
- Brachytherapy source spacer
- Model / Ref / Catalog
- 70301QC20
- Primary DI / UDI-DI
- 10801741078078
- 510(k) Number
- FDA product code
- KXK
- GMDN term
- Brachytherapy source spacer
- Device class
- Class II
- Regulation number
- 892.5730
- GUDID distribution status
- In Commercial Distribution
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