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VENTREX DATA REDUCTION & QUAL. CONTR. SY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K812357
510(k) Type
Traditional
Applicant
VENTREX LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/1/1981
Days to Decision
12 days

VENTREX DATA REDUCTION & QUAL. CONTR. SY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K812357
510(k) Type
Traditional
Applicant
VENTREX LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/1/1981
Days to Decision
12 days