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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.
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