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REVERSE MEDICAL REPORT GUIDE CATHETER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K102418
510(k) Type
Traditional
Applicant
REVERSE MEDICAL CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/2011
Days to Decision
233 days
Submission Type
Summary

REVERSE MEDICAL REPORT GUIDE CATHETER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K102418
510(k) Type
Traditional
Applicant
REVERSE MEDICAL CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/2011
Days to Decision
233 days
Submission Type
Summary