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 K033216
Device Name BZ-576 NON-INVASIVE AUTOMATIC BLOOD PRESSURE MONITOR
Applicant
THE BUZZ GROUP, LLC
PO BOX 7007
DEERFIELD,  IL  60015
Applicant Contact DANIEL KAMM, P.E.
Correspondent
THE BUZZ GROUP, LLC
PO BOX 7007
DEERFIELD,  IL  60015
Correspondent Contact DANIEL KAMM, P.E.
Regulation Number870.1130
Classification Product Code
DXN  
Date Received10/03/2003
Decision Date 05/04/2004
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Summary Summary
Type Abbreviated
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-