FDA 510(k) Applications for Medical Device Product Code: KMG (Purifier, Water, Ultraviolet, Medical)

FDA 510(k) Applications for Medical Device Product Code "KMG"
(Purifier, Water, Ultraviolet, Medical)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K012029	APOLLO CORP.	REMEDY MODEL 2Z12	12/31/2001

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