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U.S. Department of Health and Human Services

510(k) Premarket Notification
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1 to 9 of 9 Results
ProductCode: IZI Applicant: PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC. Decision Date To: 04/23/2024
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multidiagnost eleva PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC. K050151 02/09/2005
allura xper fd20 PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC. K033737 12/09/2003
philips integris allura flat detector release 1.2 PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC. K031333 05/13/2003
release 2 of philips integris series (v5000, bv5000, h5000, bh5000, hm2000) systems PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC. K984545 02/25/1999
philips integris 3d ra option PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC. K983877 12/21/1998
philips integris v5000 and bv5000 PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC. K973482 11/10/1997
ratational angiography option for philips multidiagnost 4 PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC. K971489 07/03/1997
philips integris h5000 PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC. K971365 05/14/1997
philips integris c2000 system PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC. K902542 08/17/1990
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