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CORONARY SINUS GUIDE AND LATERAL VEIN INTRODUCER KITS

Page Type
Cleared 510(K)
510(k) Number
K120158
510(k) Type
Traditional
Applicant
THOMAS MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/2012
Days to Decision
209 days
Submission Type
Summary

CORONARY SINUS GUIDE AND LATERAL VEIN INTRODUCER KITS

Page Type
Cleared 510(K)
510(k) Number
K120158
510(k) Type
Traditional
Applicant
THOMAS MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/2012
Days to Decision
209 days
Submission Type
Summary