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MICROLITE ML 1000 (MODEL 3) MICROPLATE LUMINOMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K895313
510(k) Type
Traditional
Applicant
DYNATECH LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/1989
Days to Decision
49 days

MICROLITE ML 1000 (MODEL 3) MICROPLATE LUMINOMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K895313
510(k) Type
Traditional
Applicant
DYNATECH LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/1989
Days to Decision
49 days