ZOE FLUID STATUS MONITOR— 510(k) K131509

Name: FDA 510(k) clearance K131509
Creator: U.S. Food and Drug Administration
Published: 2013-06-28

Substantially Equivalent

Noninvasive Medical Technologies, Inc.

FDA 510(k) clearance K131509 for ZOE FLUID STATUS MONITOR, Substantially Equivalent on 2013-06-28. Applicant: Noninvasive Medical Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Noninvasive Medical Technologies, Inc.
Product code: Code DSB
Device class: Class 2
Regulation: 21 CFR 870.2770
Advisory panel: Cardiovascular
Date received: 2013-05-24
Decision date: 2013-06-28
Decision: Substantially Equivalent
Clearance type: Special
Location: Las Vegas, NV, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.