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INTRAUTERINE SOUND

K935665 Class I Traditional
Decision Date
1994-02-24
Sponsor / Applicant
Rocket of London, Ltd.

Technical Specification

510(k) Submission ID K935665
Product Code HHM
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.4530
Decision Date 1994-02-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INTRAUTERINE SOUND received FDA 510(k) clearance under submission number K935665, sponsored by Rocket of London, Ltd.. 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 1994-02-24.

Classification & Regulation

This clearance is catalogued under FDA product code HHM and 21 CFR 884.4530, within the Obstetrics/Gynecology review panel as a Class I device.