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CELLECT 8E AUTOMATED BLOOD CELL COUNTERS

Page Type
Cleared 510(K)
510(k) Number
K862374
510(k) Type
Traditional
Applicant
INSTRUMENTATION LABORATORY CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/1986
Days to Decision
72 days

CELLECT 8E AUTOMATED BLOOD CELL COUNTERS

Page Type
Cleared 510(K)
510(k) Number
K862374
510(k) Type
Traditional
Applicant
INSTRUMENTATION LABORATORY CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/1986
Days to Decision
72 days