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NUK EXPRESSIVETM DOUBLE ELECTRIC BREAST PUMP

K121478 Class II Traditional
Decision Date
2013-04-05
Sponsor / Applicant
Mapa GmbH

Technical Specification

510(k) Submission ID K121478
Product Code HGX
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5160
Decision Date 2013-04-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NUK EXPRESSIVETM DOUBLE ELECTRIC BREAST PUMP received FDA 510(k) clearance under submission number K121478, sponsored by Mapa GmbH. 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 2013-04-05.

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.