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SONOTIP II ULTRASOUND NEEDLE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070129
510(k) Type
Traditional
Applicant
MEDI-GLOBE CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/2007
Days to Decision
15 days
Submission Type
Summary

SONOTIP II ULTRASOUND NEEDLE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070129
510(k) Type
Traditional
Applicant
MEDI-GLOBE CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/2007
Days to Decision
15 days
Submission Type
Summary