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HEMAGEN CRP 150 KIT (EIA METHOD)

Page Type
Cleared 510(K)
510(k) Number
K960324
510(k) Type
Traditional
Applicant
HEMAGEN DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/1996
Days to Decision
49 days
Submission Type
Summary

HEMAGEN CRP 150 KIT (EIA METHOD)

Page Type
Cleared 510(K)
510(k) Number
K960324
510(k) Type
Traditional
Applicant
HEMAGEN DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/1996
Days to Decision
49 days
Submission Type
Summary