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77 devices foundsorted by relevance

Manufacturer: The Kendal Co. Clear all

  • Kendall Curity Stomach Tubes

    The Kendal Co.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Mahurkar Triple Lumen Catheter, 12 Fr Open recall

    The Kendall Company,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Kendall Curity Urinary Drainage Bags

    The Kendal Co.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Kendall Kenguard Urinary Leg Bags

    The Kendal Co.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Curity Premium Cystoscopy Tray

    The Kendal Co.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Curity Continuous Spinal Anesthesia Tray

    The Kendal Co.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Curity I.V. Start Kit

    The Kendal Co.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Kendall Model 6325 Scd Sequel Compression System

    The Kendal Co.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Kendall Curity 100% Silicone Foley Catheter W/Temp

    The Kendal Co.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Curity Central Venous Catheter

    The Kendal Co.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Kendall Curity Intravascular Cut Down Tubes

    The Kendal Co.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Marhukar Triple Lumen Catheter, Model 12 Fr

    The Kendal Co.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Polyskin(R) M.R. Moist Responsive Transparent Dressing

    The Kendal Co.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:—

  • Monoject Insulin Syringe

    The Kendal Co.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Kendall Curity Urethral Catheters

    The Kendal Co.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Modified Model 5320 T.E.D. Compression Limb

    The Kendal Co.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Curity Silicone Nephrostomy Catheter

    The Kendal Co.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:—

Showing 61-77 of 77