FDA 510(k) Applications Submitted by CHRISTINE EHMANN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K090318	02/09/2009	CARESTREAM DRX-1 SYSTEM	CARESTREAM HEALTH, INC.
K211535	05/18/2021	Sonata Transcervical Fibroid Ablation System 2.2	Gynesonics, Inc.
K081836	06/30/2008	CARESTREAM DR LONG LENGTH IMAGING SYSTEM FOR DR 7500 SYSTEM	CARESTREAM HEALTH,INC.
K060550	03/02/2006	KODAK DIRECTVIEW DR 3000 SYSTEM 64KW/80KW GENERATORS, MODELS 6551345, 6551386	EASTMAN KODAK COMPANY
K011016	04/04/2001	LSI SOLUTIONS FLEXIBLE SUTURE PLACEMENT DEVICE AND ACCESSORIES PRODUCT	LSI SOLUTIONS
K051258	05/16/2005	KODAK DIRECTVIEW DR 7500 SYSTEM, MODEL 8791345	EASTMAN KODAK COMPANY
K051483	06/06/2005	KODAK DIRECTVIEW DR SYSTEM DETECTOR	EASTMAN KODAK COMPANY