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DYNATECH MR 300 MANUAL MICROELISA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K874244
510(k) Type
Traditional
Applicant
DYNATECH LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/1987
Days to Decision
18 days

DYNATECH MR 300 MANUAL MICROELISA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K874244
510(k) Type
Traditional
Applicant
DYNATECH LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/1987
Days to Decision
18 days