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IMMULITE 2000 SPECIFIC ALLERGENS

Page Type
Cleared 510(K)
510(k) Number
K021206
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/30/2002
Days to Decision
44 days
Submission Type
Statement

IMMULITE 2000 SPECIFIC ALLERGENS

Page Type
Cleared 510(K)
510(k) Number
K021206
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/30/2002
Days to Decision
44 days
Submission Type
Statement