DeviceClearance

MODIFICATION TO D3 ULTRA DFA RESPIRATORY VIRUS SCREENING & ID KIT— 510(k) K092300

Substantially Equivalent

Diagnostic Hybrids, Inc.

FDA 510(k) clearance K092300 for MODIFICATION TO D3 ULTRA DFA RESPIRATORY VIRUS SCREENING & ID KIT, Substantially Equivalent on 2009-08-28. 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
Special
Location
Athens, OH, US
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