K-number	K913587
Device name	JTECH 50 SERIES CUTTING LOOP
Applicant	J-Tech, Inc.
Product code	FJL
Device class	Class II
Decision date	Oct 23, 1991
Decision	Substantially Equivalent
Regulation	876.1500

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View the full FDA submission: accessdata.fda.gov

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JTECH 50 SERIES CUTTING LOOP

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