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R4 ACERT ULTRASOUND REPORTING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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