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IMMULITE HCG, MODEL LKCG1, LCCG5, IMMULITE 2000 HCG, MODEL L2KCG2, L2KCG6

Page Type
Cleared 510(K)
510(k) Number
K990222
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/1999
Days to Decision
32 days
Submission Type
Summary

IMMULITE HCG, MODEL LKCG1, LCCG5, IMMULITE 2000 HCG, MODEL L2KCG2, L2KCG6

Page Type
Cleared 510(K)
510(k) Number
K990222
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/1999
Days to Decision
32 days
Submission Type
Summary