DeviceClearance

DIAGNOSTIC HYBRIDS D3 DFA VARICELLA-ZOSTER VIRUS IDENTIFICATION KIT, 01-020000— 510(k) K070206

Substantially Equivalent

Diagnostic Hybrids, Inc.

FDA 510(k) clearance K070206 for DIAGNOSTIC HYBRIDS D3 DFA VARICELLA-ZOSTER VIRUS IDENTIFICATION KIT, 01-020000, Substantially Equivalent on 2007-08-30. Applicant: Diagnostic Hybrids, Inc..

Clearance details

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