QuickLink™, SourceLink™ 70301QC5

• FDA 510(k) K023210 decided 28 Mar 2003 Active
• FDA GUDID UDI-DI 10801741078061 listed 5 Oct 2015 Listed

1. 28 Mar 2003 Cleared FDA 510(k) K023210
2. 5 Oct 2015 Listed FDA GUDID 10801741078061

Trade name

QuickLink™, SourceLink™

Generic name

Brachytherapy source spacer

Model / Ref / Catalog

70301QC5

Primary DI / UDI-DI

10801741078061

510(k) Number

K023210 ↗

FDA product code

KXK

GMDN term

Brachytherapy source spacer

Device class

Class II

Regulation number

892.5730

GUDID distribution status

In Commercial Distribution

Category: General-purpose brachytherapy system applicator, manual,Brachytherapy source spacer

Other devices filed under FDA product code KXK (Source, brachytherapy, radionuclide).

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• CESIUM-131 STRAND, STRAND PRELOAD, PRELOAD, S-CARTRIDGE by Isoray, Inc.
• AOS MARKER SEEDS by ALPHA-OMEGA SERVICES, INC.
• PROSTEC 125I BRANCHYTHERAPY SNAPSEED by Prostec, LLC
• TheraStrand® with I-Seed XX72xiL by THERAGENICS CORP.
• North American Scientific I-125 Radionuclide Brachytherapy Source Model MED 3631-A by Ml Strategies, Inc.
• TheraSeed XX500 by THERAGENICS CORP.
• Colab Cocath Implanted Catheter and Depot by Colab Intl., Inc.
• Accu-Space Plain Gut Absorbable Seeding Spacers by Cp Medical
• Interstrand 125 & Interstrand 103, Model Numbers 1251S and 1031S by Ibt, Inc.

• BrachySource™ PS1251LS

  Class II

  FDA 510(k) K093663 Active Cleared 23 Dec 2009 GUDID on market

• BrachySource™, SourceCap™ 1251PAF

  Class II

  FDA 510(k) K140856 Active Cleared 2 May 2014 GUDID on market

• TheraSeed®, SourceLink™ 200LINKLS

  Class II

  FDA 510(k) K060636 Active Cleared 19 Apr 2006 GUDID on market

• QuickLink™, SourceLink™ 70302QC10

  Class II

  FDA 510(k) K023210 Active Cleared 28 Mar 2003 GUDID on market

See all devices from Bard Brachytherapy, Inc →