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SYSMEX R-1000 AUTOMATED RETICULOCYTE ANALYZER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K894539
510(k) Type
Traditional
Applicant
TOA MEDICAL ELECTRONICS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/1989
Days to Decision
68 days

SYSMEX R-1000 AUTOMATED RETICULOCYTE ANALYZER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K894539
510(k) Type
Traditional
Applicant
TOA MEDICAL ELECTRONICS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/1989
Days to Decision
68 days