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17 devices foundsorted by relevance

Manufacturer: Intervalve, Inc. Clear all

  • V8 V8-2328

    Intervalve, Inc.,United States(FDA applicant)
    Withdrawn Registry: GUDID Class:II

  • V8 TAV8-1924

    Intervalve, Inc.,United States(FDA applicant)
    Withdrawn Registry: GUDID Class:II

  • V8 V8-1924

    Intervalve, Inc.,United States(FDA applicant)
    Withdrawn Registry: GUDID Class:II

  • V8 TAV8-2126

    Intervalve, Inc.,United States(FDA applicant)
    Withdrawn Registry: GUDID Class:II

  • V8 172212C110

    Intervalve, Inc.,United States(FDA applicant)
    Withdrawn Registry: GUDID Class:II

  • V8 TAV8-1722

    Intervalve, Inc.,United States(FDA applicant)
    Withdrawn Registry: GUDID Class:II

  • V8 V8-2126

    Intervalve, Inc.,United States(FDA applicant)
    Withdrawn Registry: GUDID Class:II

  • V8 212612C110

    Intervalve, Inc.,United States(FDA applicant)
    Withdrawn Registry: GUDID Class:II

  • V8 TAV8-2328

    Intervalve, Inc.,United States(FDA applicant)
    Withdrawn Registry: GUDID Class:II

  • V8 V8-1722

    Intervalve, Inc.,United States(FDA applicant)
    Withdrawn Registry: GUDID Class:II

  • V8 232812C110

    Intervalve, Inc.,United States(FDA applicant)
    Withdrawn Registry: GUDID Class:II

  • V8 192412C110

    Intervalve, Inc.,United States(FDA applicant)
    Withdrawn Registry: GUDID Class:II

  • V8 Transluminal Bav Catheter

    Intervalve, Inc.,United States(FDA applicant) Group of variants
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • V8 Balloon Aortic Valvuloplasty Catheter

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

Showing 1-17 of 17