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CRYSTAL MANUAL BREAST PUMP

K850242 Class I Traditional
Decision Date
1985-02-25
Sponsor / Applicant
Crystal Medical Products, Inc.

Technical Specification

510(k) Submission ID K850242
Product Code HGY
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5150
Decision Date 1985-02-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CRYSTAL MANUAL BREAST PUMP received FDA 510(k) clearance under submission number K850242, sponsored by Crystal Medical Products, Inc.. 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 1985-02-25.

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.