FDA 510(k) Applications Submitted by DIANE M KING

FDA 510(k) Number	Submission Date	Device Name	Applicant
K061538	06/02/2006	ALARA CRYSTALVIEW COMPUTED RADIOGRAPHY SYSTEM, MODEL R200	ALARA, INC.
K222304	08/01/2022	Sonata Transcervical Fibroid Ablation System 2.2	Gynesonics, Inc.
K173703	12/04/2017	Sonata Sonography-Guided Transcervical Fibroid Ablation System	Gynesonics, Inc.
K193516	12/19/2019	Sonata« Sonography-Guided Transcervical Fibroid Ablation System 2.1	Gynesonics, Inc
K000162	01/19/2000	METRISCAN BONE DENSITY SYSTEM	ALARA, INC.
K032210	07/21/2003	ALARA CRYSTALVIEW COMPUTED RADIOGRAPHY SYSTEM	ALARA, INC.
K062390	08/16/2006	CRYSTALVIEW R200	ALARA, INC.