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SCLEROTHERAPY NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914496
510(k) Type
Traditional
Applicant
SURGITEK MEDICAL ENGINEERING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/5/1991
Days to Decision
58 days
Submission Type
Summary

SCLEROTHERAPY NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914496
510(k) Type
Traditional
Applicant
SURGITEK MEDICAL ENGINEERING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/5/1991
Days to Decision
58 days
Submission Type
Summary