FDA 510(k) Applications for Medical Device Product Code: HLZ (Electrode, Corneal)

FDA 510(k) Applications for Medical Device Product Code "HLZ"
(Electrode, Corneal)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K232273	RetMap, Inc.	RM Electrode (RMH 23-01)	12/07/2023
K961805	TOMEY CORPORATION USA	TOMEY DTL ELECTRODE	05/09/1997

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