FDA 510(k) Applications Submitted by Gynesonics, Inc

FDA 510(k) Number Submission Date Device Name Applicant
K233848 12/05/2023 Sonata Transcervical Fibroid Ablation System 2.2 (SONATA2-220) Gynesonics, Inc
K240503 02/21/2024 Sonata Transcervical Fibroid Ablation System 2.2 Gynesonics, Inc
K193516 12/19/2019 Sonata« Sonography-Guided Transcervical Fibroid Ablation System 2.1 Gynesonics, Inc


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