K-number	K843137
Device name	BP 5000
Applicant	Tech Vend Marketing
Product code	DXN
Device class	Class II
Decision date	Jan 16, 1985
Decision	Substantially Equivalent
Regulation	870.1130

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Source

View the full FDA submission: accessdata.fda.gov

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BP 5000

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