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147 devices foundsorted by relevance

Manufacturer: B&B Medical Technologies, Inc Clear all

  • Q-Cap Needle-Free Reconstitution 13mm Vial Adapter, Model 6100-01

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

  • PowerWire Radiofrequency Guidewire Kit

    Baylis Medical Technologies Inc,Canada(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Mini Heart

    B&B Medical Technologies, Inc.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Bodai M.D.D. Adaptor(Tm)

    B&B Medical Technologies, Inc.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Tympanostomy Tube

    Bluff City Medical Technologies, Inc.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • H.E.A.R.T. Nebulizer

    B&B Medical Technologies, Inc.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Heart Nebulizer Flowmeter Adaptor

    B&B Medical Technologies, Inc.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Baby E.T. Tape(Tm)

    B&B Medical Technologies, Inc.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Bmt Anscore Health Management System, Model 1.1

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

  • Collatek Sheet

    Biocore Medical Technologies, Inc.,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:—

  • Heart Nebulizer Pole Clamp

    B&B Medical Technologies, Inc.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • PowerWire® 14 Radiofrequency Guidewire Kit

    Baylis Medical Technologies Inc,Canada(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Oxy-Off(Tm)

    B&B Medical Technologies, Inc.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Modification To Bionicare Stimulator System, Model Bio-1000

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

  • Block, Bite, Intubation

    B&B Medical Technologies, Inc.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:I

  • RFP-100A Connector Cable (Single Use)

    Baylis Medical Technologies Inc,Canada(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Collatek Hydrogel

    Biocore Medical Technologies, Inc.,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:—

  • Adhesive E.T. Tape

    B&B Medical Technologies, Inc.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:I

  • PrecisePath™ Radiofrequency Puncture Generator and PrecisePath™ Footswitch

    Baylis Medical Technologies Inc,Canada(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

Showing 101-120 of 147