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13 devices foundsorted by relevance

Manufacturer: Intensive Technology, Inc. Clear all

  • Modified Ivt Peripheral Atherectomy

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

  • Ivt Introducer Sheath

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

  • Peripheral Atherectomy System

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

  • Aptt By Hemochron(R)

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

  • Modified Ivt Peripheral Atherectomy System

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

  • Hemochron(R) Heparin Response Test

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

  • Tec Rotating Dual Hemovalve

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

  • Intra-Operative Tec Atherectomy System

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

  • Respa-Trol

    Intensive Technology, Inc.,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:I

  • 0.014 Peripheral Guide Wire

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

  • Ivt 0.014 Guide Wire

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

  • Ivt Guiding Catheter

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

  • Ivt Coronary Atherectomy System (Tec)(R)

    Intensive Technology, Inc.,United States(FDA applicant)
    Withdrawn Regimes: PMA, withdrawn Registry: PMA Class:III

Showing 1-13 of 13