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Amsel Occluder Device

Page Type
Cleared 510(K)
510(k) Number
K172479
510(k) Type
Special
Applicant
Amsel Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/2017
Days to Decision
29 days
Submission Type
Statement

Amsel Occluder Device

Page Type
Cleared 510(K)
510(k) Number
K172479
510(k) Type
Special
Applicant
Amsel Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/2017
Days to Decision
29 days
Submission Type
Statement