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SCLEROTHERAPY NEEDLE

Page Type
Cleared 510(K)
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)
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