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MODIFICATION OF GIP/MEDI-GLOBE ULTRASOUND NEEDLE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990220
510(k) Type
Traditional
Applicant
MEDI-GLOBE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/1999
Days to Decision
68 days
Submission Type
Summary

MODIFICATION OF GIP/MEDI-GLOBE ULTRASOUND NEEDLE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990220
510(k) Type
Traditional
Applicant
MEDI-GLOBE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/1999
Days to Decision
68 days
Submission Type
Summary