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IMMULITE AMPHETAMINE, MODELS LKAM1, LKAM5

Page Type
Cleared 510(K)
510(k) Number
K992632
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/27/2000
Days to Decision
174 days
Submission Type
Summary

IMMULITE AMPHETAMINE, MODELS LKAM1, LKAM5

Page Type
Cleared 510(K)
510(k) Number
K992632
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/27/2000
Days to Decision
174 days
Submission Type
Summary