• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Premarket Approval (PMA)

  • 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
Note: This medical device record is a PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information.
 
DeviceSTAN S31 FETAL HEART MONITOR
Classification Nameanalyzer, data, obstetric
Generic Nameanalyzer, data, obstetric
Regulation Number884.2050
Applicant
NEOVENTA MEDICAL AB
norra agatan 32
se-431 35
molndal 
PMA NumberP020001
Supplement NumberS005
Date Received02/04/2008
Decision Date03/12/2008
Product Code
HEO[ Registered Establishments with HEO ]
Advisory Committee Obstetrics/Gynecology
Supplement Typereal-time process
Supplement Reason change design/components/specifications/material
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
APPROVAL FOR A CHANGE TO THE PATIENT INTERFACE BOX AND CABLES.
-
-