K-number	K810940
Device name	THE BETA
Applicant	Burdick Corp.
Product code	DSI
Device class	Class II
Decision date	Jul 16, 1981
Decision	Substantially Equivalent
Regulation	870.1025

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Source

View the full FDA submission: accessdata.fda.gov

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THE BETA

Everything you need for a 510(k) submission. Nothing you don't.