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EIA MONOCLONAL TOTAL IGE KIT

Page Type
Cleared 510(K)
510(k) Number
K860033
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/1986
Days to Decision
91 days

EIA MONOCLONAL TOTAL IGE KIT

Page Type
Cleared 510(K)
510(k) Number
K860033
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/1986
Days to Decision
91 days