meddevicedb.com FDA Device Reference

UTERINE VACUM ASPIRATING CURRETTE

K802360 Class II Traditional
Decision Date
1980-10-31
Sponsor / Applicant
American Hospital Supply Corp.

Technical Specification

510(k) Submission ID K802360
Product Code HHI
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5070
Decision Date 1980-10-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UTERINE VACUM ASPIRATING CURRETTE received FDA 510(k) clearance under submission number K802360, sponsored by American Hospital Supply 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 1980-10-31.

Classification & Regulation

This clearance is catalogued under FDA product code HHI and 21 CFR 884.5070, within the Obstetrics/Gynecology review panel as a Class II device.