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D3 FASTPOINT L-DFA RSV/MVP IDENTIFICATION KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093233
510(k) Type
Traditional
Applicant
DIAGNOSTIC HYBRIDS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/2009
Days to Decision
51 days
Submission Type
Summary

D3 FASTPOINT L-DFA RSV/MVP IDENTIFICATION KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093233
510(k) Type
Traditional
Applicant
DIAGNOSTIC HYBRIDS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/2009
Days to Decision
51 days
Submission Type
Summary