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LEUKOCYTE VOL. ANALYSIS APPARATUS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K802208
510(k) Type
Traditional
Applicant
COULTER ELECTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/1980
Days to Decision
6 days

LEUKOCYTE VOL. ANALYSIS APPARATUS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K802208
510(k) Type
Traditional
Applicant
COULTER ELECTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/1980
Days to Decision
6 days