meddevicedb.com FDA Device Reference

Aveta Disposable Hysteroscope

K192100 Class II Special
Decision Date
2019-12-19
Sponsor / Applicant
Meditrina, Inc.

Technical Specification

510(k) Submission ID K192100
Product Code HIH
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.1690
Decision Date 2019-12-19
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Aveta Disposable Hysteroscope received FDA 510(k) clearance under submission number K192100, sponsored by Meditrina, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2019-12-19.

Classification & Regulation

This clearance is catalogued under FDA product code HIH and 21 CFR 884.1690, within the Obstetrics/Gynecology review panel as a Class II device.