• 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.
 
DeviceIMAGE CHECKER M1000 SYSTEM
Classification Nameanalyzer,medical image
Generic Nameanalyzer,medical image
Applicant
HOLOGIC, INC.
35 crosby dr.
bedford, MA 01730
PMA NumberP970058
Supplement NumberS013
Date Received02/19/2002
Decision Date04/24/2002
Product Code
MYN[ Registered Establishments with MYN ]
Advisory Committee Radiology
Supplement Typereal-time process
Supplement Reason change design/components/specifications/material
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
APPROVAL FOR THE ADDITION OF "SMARTVIEW", A FEATURE THAT ENABLES A USER TO SEE WITH MORE DETAIL THE REGION UNDERLYING A MARKER PLACED ON A MAMMOGRAM DISPLAY.
-
-