Last synced on 9 May 2025 at 11:05 pm

D3 ULTRA DUET DFA RESPIRATORY VIRUS IDENTIFICATION KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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