Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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
-
101 to 110 of 491 Results
ProductCode: FOZ Decision Date To: 01/23/2022
 < 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 > 
Results per Page
New Search  
Export all 491 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]
instruction change for right atrial/raaf catheter QUINTON, INC. K864949 02/25/1987
cavafix(r) central venous catheter kit w/suture BURRON MEDICAL PRODUCTS, INC. K870403 05/01/1987
safeside(tm) lumed LUTHER MEDICAL PRODUCTS, INC. K871546 06/17/1987
churchill-cath CHURCHILL CORP. K872585 10/15/1987
vascular access catheter w/antimicrobial cuff C.R. BARD, INC. K873050 10/20/1987
deseret splittable catheter DESERET MEDICAL, INC. K874582 12/29/1987
j&j scalp vein infusion sets CRITIKON COMPANY,LLC K875177 01/14/1988
o.p.c. intravascular catheter TAUT, INC. K875082 03/08/1988
vitaaccess (tm) catheter introducer system VITAPHORE CORP. K872998 03/24/1988
safecath PHASE MEDICAL SYSTEMS, INC. K880260 04/19/1988
-
-