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MICRO ELISA MINI READER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K800057
510(k) Type
Traditional
Applicant
DYNATECH LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/11/1980
Days to Decision
32 days

MICRO ELISA MINI READER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K800057
510(k) Type
Traditional
Applicant
DYNATECH LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/11/1980
Days to Decision
32 days