FDA 510(k) Applications Submitted by MIKE JOHNSON, M.D.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K030782	03/11/2003	SEAMGUARD BIOABSORBABLE STAPLE LINE REINFORCEMENT MATERIAL	W. L. GORE & ASSOCIATES, INC.
K000955	03/24/2000	PLACER MODEL 6232 STEERABLE STYLET	MEDTRONIC VASCULAR
K110967	04/06/2011	ENTERPRISE ELECTROPHYSIOLOGY SYSTEM	NEURALYNX INC
K172314	08/01/2017	Ampleye Scleral RGP Lens (roflufocon D, roflufocon E, hexafocon A, paflufocon D)	Art Optical Contact Lens Inc
K032865	09/12/2003	GORE SEAMGUARD BIOABSORBABLE STAPLE LINE REINFORCEMENT MATERIAL	W. L. GORE & ASSOCIATES, INC.
K094038	12/30/2009	COMPACT TOUCH	QUANTEL S.A.
K102198	08/04/2010	COMPACT TOUCH STS	QUANTEL MEDICAL S.A.
K141063	04/24/2014	LINSCAN 808, LINSCAN 980	GME (GERMAN MEDICAL ENGINEERING) GMBH