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U.S. Department of Health and Human Services

Premarket Approval (PMA)

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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.
 
DeviceIMAGECHECKER M1000 SYSTEM
Classification Nameanalyzer,medical image
Generic Nameanalyzer,medical image
Applicant
HOLOGIC, INC.
35 crosby dr.
bedford, MA 01730
PMA NumberP970058
Supplement NumberS007
Date Received01/28/2000
Decision Date05/16/2000
Product Code
MYN[ Registered Establishments with MYN ]
Advisory Committee Radiology
Supplement Typenormal 180 day track
Supplement Reason labeling change - indications/instructions/shelf life/tradename
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for a change in labeling with respect to efficacy.
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