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R4 ACERT ULTRASOUND REPORTING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K101898
510(k) Type
Traditional
Applicant
R4, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/2011
Days to Decision
435 days
Submission Type
Summary

R4 ACERT ULTRASOUND REPORTING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K101898
510(k) Type
Traditional
Applicant
R4, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/2011
Days to Decision
435 days
Submission Type
Summary