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DIAGNOSTIC HYBRIDS D3 DFA VARICELLA-ZOSTER VIRUS IDENTIFICATION KIT, 01-020000

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070206
510(k) Type
Traditional
Applicant
Diagnostic Hybrids, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/2007
Days to Decision
220 days
Submission Type
Summary

DIAGNOSTIC HYBRIDS D3 DFA VARICELLA-ZOSTER VIRUS IDENTIFICATION KIT, 01-020000

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070206
510(k) Type
Traditional
Applicant
Diagnostic Hybrids, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/2007
Days to Decision
220 days
Submission Type
Summary