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IMMULITE (HPL) (HUMAN PLACENTAL PLACTOGEN)

Page Type
Cleared 510(K)
510(k) Number
K944933
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/10/1995
Days to Decision
155 days
Submission Type
Summary

IMMULITE (HPL) (HUMAN PLACENTAL PLACTOGEN)

Page Type
Cleared 510(K)
510(k) Number
K944933
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/10/1995
Days to Decision
155 days
Submission Type
Summary