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REFLEX BALLON GUIDE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K112262
510(k) Type
Traditional
Applicant
Reverse Medical Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/2/2011
Days to Decision
86 days
Submission Type
Summary

REFLEX BALLON GUIDE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K112262
510(k) Type
Traditional
Applicant
Reverse Medical Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/2/2011
Days to Decision
86 days
Submission Type
Summary