• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification

  • Print
  • Share
  • E-mail
-
1 to 4 of 4 Results
ProductCode: OWB Applicant: PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC. Decision Date To: 05/29/2024
Results per Page
New Search  
Export all 4 Records to ExcelExport to Excel | Download Files | More About 510(k)
Device Name
Sort by Device Name [A-Z]
Sort by Device Name [Z-A]
Applicant
Sort by Applicant [A-Z]
Sort by Applicant [Z-A]
510(K)
Number
Sort by 510(k) Number [0-9]
Sort by 510(k) Number [9-0]
Decision
Date
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
allura xper or table series PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC. K102005 08/09/2010
allura xper fd20 PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC. K033737 12/09/2003
philips integris allura PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC. K002016 09/06/2000
philips duo diagnost PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC. K983069 11/02/1998
-
-