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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 supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.
 
Device MedMira Rapid HIV Test
Classification Nametest, hiv detection
Generic Namehiv detection test
Regulation Number866.3956
Applicant
MedMira Labs
155 chain lake drive, bayers lake
Halifax 
nova scotia CA B3S 1B3
PMA NumberBP000023
Supplement NumberS032
Date Received05/08/2007
Decision Date06/04/2007
Decision Approved
Product Code
MZF[ Registered Establishments with MZF ]
Advisory Committee Microbiology
Supplement Type30-Day Notice
Expedited Review Granted? No
Third Party Review Elligble? No
Combination ProductNo
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