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ROTALEX 2 LATEX AGGLUTINATION TEST FOR ROTAVIRUS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K854129
510(k) Type
Traditional
Applicant
ORION DIAGNOSTICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/21/1986
Days to Decision
104 days

ROTALEX 2 LATEX AGGLUTINATION TEST FOR ROTAVIRUS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K854129
510(k) Type
Traditional
Applicant
ORION DIAGNOSTICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/21/1986
Days to Decision
104 days