• 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 500 Results *
Decision Date To: 05/21/2019
Results per Page
New Search  
Export all 500 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]
Sort by Applicant [A-Z]
Sort by Applicant [Z-A]
Sort by 510(k) Number [0-9]
Sort by 510(k) Number [9-0]
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
(.o38) hi-torque guide wires TARGET THERAPEUTICS K860533 03/31/1986
(1) digital blood pressure monitor, model md-250; (2) fully automatic blood pressure monitor, model md-700 MEDITEC CO., LTD. K990380 02/22/1999
(125 i) digitoxin ria kit DIAGNOSTIC PRODUCTS CORP. K780766 07/27/1978
(125i) htsh radioimmunoassay kit YANG LABORATORIES, INC. K821620 06/14/1982
(125i) testosterone kit RADIOASSAY SYSTEMS LABORATORIES, INC. K791999 10/30/1979
(ast) or (alt) uv determ. phy. phos. THE DOW CHEMICAL CO. K781020 07/27/1978
(brand name) LONG IN TIME ENT. CO., LTD. K971384 07/01/1997
(brand name) sunglass frames CUSTOM OPTICAL FRAMES, INC. K962478 07/25/1996
(brand name0 mondain CHAN'S PLASTIC MANUFACTORY CO., LTD. K943840 09/06/1994
(calas(tm)) w/add'l reagent calas(tm) pronase MERIDIAN DIAGNOSTICS, INC. K894845 09/08/1989

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.