meddevicedb.com FDA Device Reference

BELFORT-DILDY OBSTETRIC TAMPONADE SYSTEM

K091958 Class II Traditional
Decision Date
2010-04-30
Sponsor / Applicant
Glenveigh Surgical, LLC

Technical Specification

510(k) Submission ID K091958
Product Code OQY
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.4530
Decision Date 2010-04-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BELFORT-DILDY OBSTETRIC TAMPONADE SYSTEM received FDA 510(k) clearance under submission number K091958, sponsored by Glenveigh Surgical, LLC. 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 2010-04-30.

Classification & Regulation

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