meddevicedb.com FDA Device Reference

RESUSCITATOR'S GUARD SUCTION CONTROL SYSTEM

K884917 Class II Traditional
Decision Date
1989-03-09
Sponsor / Applicant
Amg Medical Equipments, Inc.

Technical Specification

510(k) Submission ID K884917
Product Code IZH
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1710
Decision Date 1989-03-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RESUSCITATOR'S GUARD SUCTION CONTROL SYSTEM received FDA 510(k) clearance under submission number K884917, sponsored by Amg Medical Equipments, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1989-03-09.

Classification & Regulation

This clearance is catalogued under FDA product code IZH and 21 CFR 892.1710, within the Radiology review panel as a Class II device.