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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.
 
Trade NameCOBAS HPV TEST
Classification Namekit, dna detection, human papillomavirus
Generic Namehuman papillomavirus dna test detection kit
ApplicantROCHE MOLECULAR SYSTEMS, INC.
PMA NumberP100020
Supplement NumberS001
Date Received05/31/2011
Decision Date12/29/2011
Product Code
MAQ[ Registered Establishments with MAQ ]
Advisory Committee Microbiology
Supplement Typenormal 180 day track no user fee
Supplement Reason location change: manufacturer
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for a manufacturing site located at roche molecular systems, inc. In somerville, new jersey.
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