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SONIXGPS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121812
510(k) Type
Traditional
Applicant
UltraSonix Medical Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/2013
Days to Decision
530 days
Submission Type
Statement

SONIXGPS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121812
510(k) Type
Traditional
Applicant
UltraSonix Medical Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/2013
Days to Decision
530 days
Submission Type
Statement