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SYSMEX DD-100 WHOLE BLOOD DILUTION SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882767
510(k) Type
Traditional
Applicant
TOA MEDICAL ELECTRONICS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/1988
Days to Decision
12 days

SYSMEX DD-100 WHOLE BLOOD DILUTION SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882767
510(k) Type
Traditional
Applicant
TOA MEDICAL ELECTRONICS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/1988
Days to Decision
12 days