DeviceClearance

D3 DUET DFA INFLUENZA A/RESPIRATORY VIRUS SCREENING KIT— 510(k) K081746

Substantially Equivalent

Diagnostic Hybrids, Inc.

FDA 510(k) clearance K081746 for D3 DUET DFA INFLUENZA A/RESPIRATORY VIRUS SCREENING KIT, Substantially Equivalent on 2008-12-23. Applicant: Diagnostic Hybrids, Inc..

Clearance details

Applicant
Diagnostic Hybrids, Inc.
Product code
Code GNW
Advisory panel
Microbiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Athens, OH, US
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