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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
K051247
510(k) Type
Special
Applicant
MEDI-GLOBE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/2005
Days to Decision
31 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
K051247
510(k) Type
Special
Applicant
MEDI-GLOBE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/2005
Days to Decision
31 days
Submission Type
Summary