K-number	K901612
Device name	VITALMAX 2000 ECG MONITOR W/NON-INVASIVE BLOOD-PRE
Applicant	Pace Tech, Inc.
Product code	DQA
Device class	Class II
Decision date	Apr 30, 1990
Decision	Substantially Equivalent
Regulation	870.2700

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View the full FDA submission: accessdata.fda.gov

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VITALMAX 2000 ECG MONITOR W/NON-INVASIVE BLOOD-PRE

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