meddevicedb.com FDA Device Reference

AXICARE BREAST PUMP MODEL

K811403 Class II Traditional
Decision Date
1981-06-12
Sponsor / Applicant
Neonatal Corp.

Technical Specification

510(k) Submission ID K811403
Product Code HGX
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5160
Decision Date 1981-06-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AXICARE BREAST PUMP MODEL received FDA 510(k) clearance under submission number K811403, sponsored by Neonatal Corp.. 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 1981-06-12.

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.