K-number	K142583
Device name	LaborView LV1000
Applicant	Obmedical Company
Product code	OSP
Device class	Class II
Decision date	Jan 16, 2015
Decision	Substantially Equivalent
Regulation	884.2720

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Source

View the full FDA submission: accessdata.fda.gov

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LaborView LV1000

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