FDA 510(k) Applications for Medical Device Product Code: KCX (Epilator, High Frequency, Tweezer-Type)

FDA 510(k) Applications for Medical Device Product Code "KCX"
(Epilator, High Frequency, Tweezer-Type)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K973179	GLOBAL TV CONCEPTS, LTD.	FEMINIQUE SONIC HAIR REMOVER	10/30/1997
K973174	GLOBAL TV CONCEPTS, LTD.	SONIQUE HAIR REMOVER	10/30/1997
K970338	IGIA DIRECT, INC.	TWEEZER-TYPE EPILATOR	07/01/1997
K972695	MEHL/GROUP MARKETING	FINALLY FREE	10/22/1997
K973340	MOBIT, INC.	TWEEZER-TYPE EPILATOR	12/03/1997
K935706	UNIVERSAL H.R. SYSTEM, INC.	EPI 2	02/11/1997
K973773	WELLQUEST INTL., INC.	DAPELLE HAIR REMOVER	12/17/1997