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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name real time nucleic acid amplification system
510(k) Number K170558
Device Name revogene
Applicant
GenePOC Inc.
360 rue Franquet
Quebec,  CA G1P 4N3
Applicant Contact Guy Sevigny
Correspondent
GenePOC Inc.
360 rue Franquet
Quebec,  CA G1P 4N3
Correspondent Contact Guy Sevigny
Regulation Number862.2570
Classification Product Code
OOI  
Date Received02/24/2017
Decision Date 05/25/2017
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Microbiology
Summary Summary
FDA Review Decision Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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