• 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
-
81 to 90 of 500 Results *
 < 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 16 
 17 
 > 
results per page
New Searchexport reports to excelExport to Excel | HelpHelp
Device Name
Sort by Device Name [A-Z]
Sort by Device Name [Z-A]
Applicant
Sort by PMA Number [0-9]
Sort by PMA Number [9-0]
510(K)
Number
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
Decision
Date
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
hawkins electrokinetic body activating LEISURE WAY k820938 06/11/1982
venoset dual-rate piggyback w/ivex & ABBOTT LABORATORIES k821578 06/22/1982
hemodialysis system FHK k813432 06/23/1982
hollow fiber dialyzers TERUMO MEDICAL CORP. k820743 06/23/1982
scanner type 1846 BRUEL & KJAER INSTRUMENTS, INC. k827380 07/09/1982
pregnancy (w) edge BODY THERAPEUTICS, INC. k821836 07/30/1982
the ocuplot d COHERENT MEDICAL DIVISION k822415 09/07/1982
toxoplasma gondii antibody igg IMMULOK, INC. k822605 10/27/1982
heavy-duty i.v. stand E.F. BREWER CO. k823270 11/17/1982
press-o-test MEDI-SWISS CORP. k822102 11/24/1982

*   The maximum 500 records meeting your search criteria returned. Please narrow your search.
-
-