Last synced on 18 April 2025 at 11:05 pm

REVERSE MEDICAL REPORT GUIDE CATHETER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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