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K-ASSAY TOTAL IGE, K-ASSAY IGE CALIBRATOR SET, MODELS KAI-092/KAI-093C

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K042241
510(k) Type
Traditional
Applicant
KAMIYA BIOMEDICAL CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/2004
Days to Decision
113 days
Submission Type
Statement

K-ASSAY TOTAL IGE, K-ASSAY IGE CALIBRATOR SET, MODELS KAI-092/KAI-093C

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K042241
510(k) Type
Traditional
Applicant
KAMIYA BIOMEDICAL CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/2004
Days to Decision
113 days
Submission Type
Statement