meddevicedb.com FDA Device Reference

BAG DECANTER

K852777 Class II Traditional
Decision Date
1985-08-16
Sponsor / Applicant
Advance Medical Designs, Inc.

Technical Specification

510(k) Submission ID K852777
Product Code KPE
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5025
Decision Date 1985-08-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BAG DECANTER received FDA 510(k) clearance under submission number K852777, sponsored by Advance Medical Designs, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1985-08-16.

Classification & Regulation

This clearance is catalogued under FDA product code KPE and 21 CFR 880.5025, within the General Hospital review panel as a Class II device.