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D3 ULTRA DUET DFA RESPIRATORY VIRUS IDENTIFICATION KIT

Page Type
Cleared 510(K)
510(k) Number
K091171
510(k) Type
Traditional
Applicant
Diagnostic Hybrids, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/2009
Days to Decision
142 days
Submission Type
Summary

D3 ULTRA DUET DFA RESPIRATORY VIRUS IDENTIFICATION KIT

Page Type
Cleared 510(K)
510(k) Number
K091171
510(k) Type
Traditional
Applicant
Diagnostic Hybrids, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/2009
Days to Decision
142 days
Submission Type
Summary