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UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, D.C. 20549SCHEDULE 14A INFORMATION Proxy Statement Pursuant to Section 14(a) of the Securities Exchange Act of 1934 (Amendment No. ) Filed
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View PDF - Viveve is a document that provides detailed information about the Viveve medical device.
Manufacturers and distributors of the Viveve medical device are required to file the View PDF - Viveve document.
The View PDF - Viveve document can be filled out electronically on the FDA's website.
The purpose of the View PDF - Viveve document is to provide essential information about the Viveve medical device to regulatory authorities.
The View PDF - Viveve must include details about the device design, materials, intended use, and any clinical studies conducted.
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