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RAPID DIRECT STREP A LATEX AGGLUTINATION TEST

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K852841
510(k) Type
Traditional
Applicant
SMITH KLINE DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/24/1985
Days to Decision
19 days

RAPID DIRECT STREP A LATEX AGGLUTINATION TEST

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K852841
510(k) Type
Traditional
Applicant
SMITH KLINE DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/24/1985
Days to Decision
19 days