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56 devices foundsorted by relevance

Manufacturer: Dlp, Inc. Clear all

  • Cardiopulminary Bypass Catheter Cannula

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

  • Adapters-Y-Type

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

  • Catheter Two Stage Venous Return

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

  • Contain-Or

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

  • Touriquet Kit With Snare Open recall

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

  • Lancaster Cooling Jacket, Cat. Code #13500/13501

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

  • Intracardiac Sump 12010 Open recall

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

  • Pressure Display Box #60000/Tubing Set #61000

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

  • Electro-Cautery Knife Cleaner 6000 1

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

  • Coronary Ostium Occluder, Catalog Code 32015

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

  • Cuatico Myelography Needles

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

  • Aortic Root Cannula Open recall

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

  • Octopus Tissue Stabilizer (28001/28002/28003/28004/28005/28006)

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

  • Cardiopulmonary Bypass Open recall

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

  • Maxx 470 Core Biopsy Gun

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

  • Angiography Needle W/Wo Connection

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

Showing 41-56 of 56