K-number	K800022
Device name	MODEL 807 SUCTION CAUTERY FINGER TIP
Applicant	Malibu Laboratories
Product code	GEI
Device class	Class II
Decision date	Feb 11, 1980
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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MODEL 807 SUCTION CAUTERY FINGER TIP

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