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FDA Device Info: PASs submitted by Atricure, Inc.
FDA Device Info: PASs submitted by Atricure, Inc.
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Request: All PMA-related annual reports submitted by Atricure, Inc. to the FDA from the period of Jan 2010 to the present, related to any and all of the Company`s products. Also requesting copies of the post-approval study reports (PASs) submitted by the Company to the FDA related to these same products.
Request Year: 2019
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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