K-number	K053578
Device name	SCORPION ULTRASONIC SCALING INSERTS
Applicant	Scorpion
Product code	ELC
Device class	Class II
Decision date	Jul 14, 2006
Decision	Substantially Equivalent
Regulation	872.4850

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View the full FDA submission: accessdata.fda.gov

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SCORPION ULTRASONIC SCALING INSERTS

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