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17 devices foundsorted by relevance

  • Rubella Igg Eia Test Kit

    Labsystems, Inc.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Resubmitted Fecatwin Sensitive - Feca-Eia

    Labsystems, Inc.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Labsystems Fp-901 Chemistry Analyzer

    Labsystems, Inc.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Rubella Igm Eia Test Kit

    Labsystems, Inc.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Modified Labysystems' Toxoplasma Gondii Igg Eia

    Labsystems, Inc.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Tilt/Reduced Shear Semi-Recline Seating System

    Labsystems, Inc.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Toxoplasma Gondii Igg Eia Test Kit (Amendment)

    Labsystems, Inc.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Labsystems Uniskan

    Labsystems, Inc.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Modified Labsystems' Rubella Igg Eia Test Kit

    Labsystems, Inc.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Toxoplasma Gondii Igm Eia Test Kit

    Labsystems, Inc.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Modified Toxoplasma Gondii Igg Eia Test Kit

    Labsystems, Inc.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Toxoplasma Gond Ii Igg Dia Test Kit

    Labsystems, Inc.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Rubella Igg - Eia Test Kit Number 61 07 201

    Labsystems, Inc.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Cytomegalovirus Igg Eia Test Kit

    Labsystems, Inc.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Modification Rubella Igm Eia Test Kit

    Labsystems, Inc.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Auto-Eia

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

Showing 1-17 of 17