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Monogram Technologies Provides 510(k) Submission Update Following FDA Meeting; Application Passed Initial FDA Review; Received Additional Information Request From FDA; FDA Placed Hold Pending Complete Response To AIR

Author: Benzinga Newsdesk | December 18, 2024 08:40am

Management Anticipates That it has Sufficiently Addressed the FDA's Concerns to Mitigate the Need for a Clinical Data Request

Management Anticipates a Comprehensive AIR Response in Q1 2025

Posted In: MGRM