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FDA 510(k) Applications Submitted by Golden Stapler Surgical Co., Ltd.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K162707
09/28/2016
Single Use Circular Stapler, Single Use Hemorrhoidal Circular Stapler, Single Patient Use Linear Stapler and Reload, Single Patient Use Linear Cutter and Reload, Single Patient Use Endo Cutter and Reload, Single Patient Use Transverse Cutter and Reload
Golden Stapler Surgical Co., Ltd.
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