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UNIMAX VERESS NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K111441
510(k) Type
Traditional
Applicant
UNIMAX MEDICAL SYSTEMS, INC.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
8/19/2011
Days to Decision
87 days
Submission Type
Summary

UNIMAX VERESS NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K111441
510(k) Type
Traditional
Applicant
UNIMAX MEDICAL SYSTEMS, INC.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
8/19/2011
Days to Decision
87 days
Submission Type
Summary