meddevicedb.com FDA Device Reference

BEMIS TWO GALLON CHEMOTHERAPY CONTAINER

K964858 Class II Traditional
Decision Date
1997-02-11
Sponsor / Applicant
Bemis Mfg. Co.

Technical Specification

510(k) Submission ID K964858
Product Code MMK
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5570
Decision Date 1997-02-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BEMIS TWO GALLON CHEMOTHERAPY CONTAINER received FDA 510(k) clearance under submission number K964858, sponsored by Bemis Mfg. Co.. 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 1997-02-11.

Classification & Regulation

This clearance is catalogued under FDA product code MMK and 21 CFR 880.5570, within the General Hospital review panel as a Class II device.