D3 ULTRA DFA RESPIRATORY VIRUS SCREENING & ID KIT— 510(k) K061101

Substantially Equivalent

Diagnostic Hybrids, Inc.

FDA 510(k) clearance K061101 for D3 ULTRA DFA RESPIRATORY VIRUS SCREENING & ID KIT, Substantially Equivalent on 2006-11-20. Applicant: Diagnostic Hybrids, Inc..

Clearance details

Applicant: Diagnostic Hybrids, Inc.
Product code: Code GNW
Advisory panel: Microbiology
Date received: 2006-04-20
Decision date: 2006-11-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Athens, OH, US

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