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Re: trusttheman post# 13442

Saturday, 04/06/2024 5:06:46 AM

Saturday, April 06, 2024 5:06:46 AM

Post# of 13622
Totally agree! FDA has had the PMA in inventory and worked on two or more occasions. No need to reinvent the wheel.
The FDA has been here and knows UEEC well! "In anticipation of re-submitting updated PMA information, UHP has engaged regularly with the FDA. Through this engagement the Company was recently notified that it had been selected as the first medical device application for Premarket Approval (PMA) to be submitted and evaluated using the FDA’s electronic Submission Template and Resource (“e-STAR”) platform."
$5-$10++
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