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
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name System, Measurement, Blood-Pressure, Non-Invasive
510(k) Number K080289
Device Name 1500 PRO
Applicant
Omron Healthcare, Inc.
3460 Pointe Creek Court #102
Bonita Springs,  FL  34134
Applicant Contact PAUL DRYDEN
Correspondent
Omron Healthcare, Inc.
3460 Pointe Creek Court #102
Bonita Springs,  FL  34134
Correspondent Contact PAUL DRYDEN
Regulation Number870.1130
Classification Product Code
DXN  
Date Received02/04/2008
Decision Date 02/26/2008
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-