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HUMAN PLACENTAL LACTOGEN KIT

Page Type
Cleared 510(K)
510(k) Number
K823201
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/29/1982
Days to Decision
34 days

HUMAN PLACENTAL LACTOGEN KIT

Page Type
Cleared 510(K)
510(k) Number
K823201
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/29/1982
Days to Decision
34 days