Skip to content

Results for “”

Registry
Country / market
Risk class
More classes (11)
Verified

Category (EMDN)

Browse by category
Reset

12 devices foundsorted by relevance

Manufacturer: Cardima, Inc. Clear all

  • Cardima Vueport Coronary Sinus Balloon Occlusion Guiding Catheter

    Cardima, Inc.,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Naviport Deflectable Tip Guiding Catheter

    Cardima, Inc.,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Tracer O-T-W Mapping Device

    Cardima, Inc.,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Electrode Switchbox, Model 11-081002

    Cardima, Inc.,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Modification To: Cardima Ablation System

    Cardima, Inc.,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Pathfinder

    Cardima, Inc.,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Cardima Pathfinder 1.5F Mapping Microcatheter

    Cardima, Inc.,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Cardima Seeker And Stubbie Guidewires

    Cardima, Inc.,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Cardima Tracker(R) Infusion Catheter

    Cardima, Inc.,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Forerunner

    Cardima, Inc.,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Pathfinder 3mm Mapping Microcatheter (01-082001)

    Cardima, Inc.,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Cardima Ablation System

    Cardima, Inc.,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

Showing 1-12 of 12