Birthnet Ii Perinatal Patient Data Management System

• • Terminated Z-0115-06 FDA Unclassified (pre-2012) ·initiated 13 Oct 2005

  Potential for incorrect weight to be displayed.

510(k) Number

K965008 ↗

FDA Product Code

HGM

Device Class

Class II

Regulation

21 CFR Part 884.2740

Advisory Committee

Obstetrics/Gynecology

FDA Decision

SESE Substantially Equivalent

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