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AMSEL OCCLUDER DEVICE

Page Type
Cleared 510(K)
510(k) Number
K140932
510(k) Type
Traditional
Applicant
AMSEL MEDICAL CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/2015
Days to Decision
287 days
Submission Type
Summary

AMSEL OCCLUDER DEVICE

Page Type
Cleared 510(K)
510(k) Number
K140932
510(k) Type
Traditional
Applicant
AMSEL MEDICAL CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/2015
Days to Decision
287 days
Submission Type
Summary