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Catheter Research C/O Burditt, Bowles & Radzius

Country not established

Devices
8

What Catheter Research C/O Burditt, Bowles & Radzius makes

The company manufactures steerable catheters, including the CRI CYNOSAR CATHETER, designed for vascular procedures, alongside vessel occlusion systems like the CRI OCCLUSION COIL for embolization. It also produces micro-guide systems for precise catheter navigation and electronic control systems for catheter manipulation, such as the CRI STEERABLE CATHETER CONTROL SYSTEM.

These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States and its products are listed in the FDA’s 510(k) registry.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue8

Newest first, rows 1-8 of 8

  • Cri Cynosar Catheter Ref K904785

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Cri Steerable Catheter Control System Ref K904787

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Cri Vessel Occlusin System/Cri Occlusion Coil Ref K914523

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Micro-Guide Ref K870700

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Cri Electronic Control System Ref K924125

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Cri Cynosar Catheter Ref K900320

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Cri Cynosar Catheter Ref K924227

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Micro-Guide System Ref K884337

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Catheter Research C/O Burditt, Bowles & Radzius have in the registry?

The registry currently lists 8 devices for Catheter Research C/O Burditt, Bowles & Radzius. Devices recorded under merged duplicate company entries are counted once.

Which registries list Catheter Research C/O Burditt, Bowles & Radzius's devices?

Among its 8 most recently registered devices, Catheter Research C/O Burditt, Bowles & Radzius has devices listed in FDA 510(k) (8 devices).

What risk classes do Catheter Research C/O Burditt, Bowles & Radzius's devices fall under?

Among its 8 most recently registered devices, the classes recorded for Catheter Research C/O Burditt, Bowles & Radzius's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Catheter Research C/O Burditt, Bowles & Radzius in the registry?

The most recently registered devices listed for Catheter Research C/O Burditt, Bowles & Radzius include CRI CYNOSAR CATHETER, CRI STEERABLE CATHETER CONTROL SYSTEM, CRI VESSEL OCCLUSIN SYSTEM/CRI OCCLUSION COIL and MICRO-GUIDE.

Generated automatically from registry data and not verified by a human reviewer.