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PTFE SUPER SHEATH INTRODUCER

Page Type
Cleared 510(K)
510(k) Number
K130855
510(k) Type
Traditional
Applicant
MARTECH MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/2013
Days to Decision
123 days
Submission Type
Summary

PTFE SUPER SHEATH INTRODUCER

Page Type
Cleared 510(K)
510(k) Number
K130855
510(k) Type
Traditional
Applicant
MARTECH MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/2013
Days to Decision
123 days
Submission Type
Summary