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LIQUI-HEME HEMOGLOBIN CALIBRATORS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K842668
510(k) Type
Traditional
Applicant
BIO DIAGNOSTIC INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/1985
Days to Decision
238 days

LIQUI-HEME HEMOGLOBIN CALIBRATORS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K842668
510(k) Type
Traditional
Applicant
BIO DIAGNOSTIC INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/1985
Days to Decision
238 days