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U.S. Department of Health and Human Services

510(K) Premarket Notification
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161 to 170 of 500 Results *
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Device Name
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Applicant
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510(K)
Number
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Decision
Date
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omnicare dental implant system OMNICARE DENTAL IMPLANT CENTER k000035 09/28/2001
omni grace nitrile, blue, examination glove, powder-free, polymer coated OMNIGRACE LTD. k994246 01/31/2000
olympus hdl cholesterol reagent; olympus hdl cholesterol calibrator; olympus hdl/ldl cholesterol control sera OLYMPUS AMERICA, INC. k014015 02/08/2002
olympus creatine kinase reagent osr6179/6279 OLYMPUS DIAGNOSTICA GMBH k994189 01/20/2000
ois-stand alone diagnostic ultrasound system OPTIMAL IMAGING SYSTEMS, INC. k000034 02/24/2000
ocular sciences, inc. biomedics uv asphere (ocufilcon d) soft (hydrophilic) contact lens CL MCINTOSH k020193 02/28/2002
numed mullins pta catheter NUMED, INC. k013601 01/03/2002
nucleotomy intradiscal catheter ORATEC INTERVENTIONS, INC. k013622 01/31/2002
nt meditens plus, type 290 BIO-MEDICAL RESEARCH, LTD. k014020 07/11/2002
novabone-bioglass bone graft particulate U.S. BIOMATERIALS CORP. k000149 02/07/2000

*   The maximum 500 records meeting your search criteria returned. Please narrow your search.
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