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K-ASSAY APO A1/B CALIBRATOR SET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993606
510(k) Type
Traditional
Applicant
KAMIYA BIOMEDICAL CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/26/1999
Days to Decision
32 days
Submission Type
Statement

K-ASSAY APO A1/B CALIBRATOR SET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993606
510(k) Type
Traditional
Applicant
KAMIYA BIOMEDICAL CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/26/1999
Days to Decision
32 days
Submission Type
Statement