meddevicedb.com FDA Device Reference

NURTURE III

K924312 Class II Traditional
Decision Date
1995-05-11
Sponsor / Applicant
Bailey Medical Engineering

Technical Specification

510(k) Submission ID K924312
Product Code HGX
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5160
Decision Date 1995-05-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NURTURE III received FDA 510(k) clearance under submission number K924312, sponsored by Bailey Medical Engineering. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 1995-05-11.

Classification & Regulation

This clearance is catalogued under FDA product code HGX and 21 CFR 884.5160, within the Obstetrics/Gynecology review panel as a Class II device.