K-number	K893389
Device name	MODEL SE-5 EPILATOR
Applicant	R. A. Fischer Co. Corp.
Product code	KCW
Device class	Class I
Decision date	Jun 5, 1989
Decision	Substantially Equivalent
Regulation	878.5350

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View the full FDA submission: accessdata.fda.gov

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MODEL SE-5 EPILATOR

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