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GYRUS ACMI BIOCOAG PROBE

Page Type
Cleared 510(K)
510(k) Number
K092571
510(k) Type
Traditional
Applicant
GYRUS ACMI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/20/2010
Days to Decision
425 days
Submission Type
Summary

GYRUS ACMI BIOCOAG PROBE

Page Type
Cleared 510(K)
510(k) Number
K092571
510(k) Type
Traditional
Applicant
GYRUS ACMI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/20/2010
Days to Decision
425 days
Submission Type
Summary