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IMMULITE HCG HIGH LEVEL CONTROL MODULE

Page Type
Cleared 510(K)
510(k) Number
K952251
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/1995
Days to Decision
116 days
Submission Type
Summary

IMMULITE HCG HIGH LEVEL CONTROL MODULE

Page Type
Cleared 510(K)
510(k) Number
K952251
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/1995
Days to Decision
116 days
Submission Type
Summary