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AUTODILUTER III

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K810659
510(k) Type
Traditional
Applicant
DYNATECH CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/1981
Days to Decision
20 days

AUTODILUTER III

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K810659
510(k) Type
Traditional
Applicant
DYNATECH CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/1981
Days to Decision
20 days