FDA 510(k) Applications for Medical Device Product Code: OTZ ()

FDA 510(k) Applications for Medical Device Product Code "OTZ"

FDA 510(k) Number	Applicant	Device Name	Decision Date
K203586	CorneaGen, Inc	EndoSerter-PL	02/02/2022
K110734	FISCHER SURGICAL INC.	NCI SPATULA	05/31/2012
K102999	KANEKA CORP.	TRIMOTION INJECTOR	12/29/2011
K090626	OCULAR SYSTEMS, INC.	ENDOSERTER	01/21/2011
K121579	TDAK MEDICAL, INC	EK DELIVERY DEVICE	10/03/2012

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