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Meditech International, Inc.

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K081355	BIOFLEX LD-R100 TREATMENT HEAD	ILY	2008-12-18	View
510(k)	K072551	LD-I 75 AND LD-I 200	NHN	2008-04-02	View
510(k)	K051875	BIOFLEX PRESCRIPTION SYSTEM AND RELATED TREATMENT HEADS	ILY	2006-03-13	View
510(k)	K041885	BIOFLEX LD-175 AND LD-1200 TREATMENT HEADS	ILY	2005-02-24	View
510(k)	K023621	BIOFLEX PROFESSIONAL THERAPY SYSTEM	ILY	2003-04-10	View

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