K-number	K852683
Device name	ELECTROSURGICAL LATERAL RELEASE PROBE MOD ALR-100
Applicant	American Bentley
Product code	GEI
Device class	Class II
Decision date	Aug 12, 1985
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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ELECTROSURGICAL LATERAL RELEASE PROBE MOD ALR-100

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