FDA 510(k) Applications for Medical Device Product Code: LXP (Plug, Scleral)

FDA 510(k) Applications for Medical Device Product Code "LXP"
(Plug, Scleral)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K022186	MICROVISION, INC.	SCLERAL PLUGS, 19 AND 20 GAUGE	02/26/2003
K990872	OPHTHALMIC CONSULTANTS, INC.	SCLERAL PLUGS, 19 AND 20 GAUGE	07/13/1999

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