meddevicedb.com FDA Device Reference

SECURE EVA DUAL CHAMBER MIXING BAG

K960581 Class II Traditional
Decision Date
1996-04-30
Sponsor / Applicant
Secure Medical Products, Inc.

Technical Specification

510(k) Submission ID K960581
Product Code KPE
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5025
Decision Date 1996-04-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SECURE EVA DUAL CHAMBER MIXING BAG received FDA 510(k) clearance under submission number K960581, sponsored by Secure Medical Products, 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 1996-04-30.

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.