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WHITE RIVER MANUAL BREAST PUMP

K925738 Class I Traditional
Decision Date
1994-05-04
Sponsor / Applicant
White River (Tm)

Technical Specification

510(k) Submission ID K925738
Product Code HGY
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5150
Decision Date 1994-05-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WHITE RIVER MANUAL BREAST PUMP received FDA 510(k) clearance under submission number K925738, sponsored by White River (Tm). 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 1994-05-04.

Classification & Regulation

This clearance is catalogued under FDA product code HGY and 21 CFR 884.5150, within the Obstetrics/Gynecology review panel as a Class I device.