• 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: FDF Applicant: PENTAX MEDICAL COMPANY Decision Date To: 05/01/2024
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]
pentax video colonoscopes (ec family) PENTAX MEDICAL COMPANY K131855 04/09/2014
pentex ec-3890li PENTAX MEDICAL COMPANY K093037 12/28/2009
ec-3870cilk, confocal video colonoscope PENTAX MEDICAL COMPANY K042741 10/19/2004
isc-1000 pentax confocal laser system PENTAX MEDICAL COMPANY K042740 10/19/2004
-
-