• 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 9 of 9 Results
ProductCode: FOZ Applicant: ARROW INTL., INC Decision Date To: 07/28/2014
Results per Page
New Search
Export all 9 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]
ac 3 lumen central venous access kit wit arrow intl., inc. K032962 10/29/2003
mac two-lumen central venous kit with ar arrow intl., inc. K011761 10/31/2001
two-lumen central venous access kit with arrow intl., inc. K002507 03/21/2001
arrowg +ard blue plus antimicrobial mult arrow intl., inc. K993691 03/08/2000
arrow-howes large bore multi-lumen centr arrow intl., inc. K970864 10/17/1997
arrowgard blue quad-lumen central venous arrow intl., inc. K962577 08/21/1997
arrow blood containment device arrow intl., inc. K924558 08/19/1993
antimicrobial multi-lumen central venous arrow intl., inc. K900263 07/24/1990
arrow 18ga two-lumen intravenous cath/23 arrow intl., inc. K862153 12/11/1986
-
-