meddevicedb.com FDA Device Reference

SWANK BLOOD TRANSFUSION MICRO-FILTER W/STRAIGHT SE

K855064 Class II Traditional
Decision Date
1986-03-12
Sponsor / Applicant
Cobe Laboratories, Inc.

Technical Specification

510(k) Submission ID K855064
Product Code CAK
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 1986-03-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SWANK BLOOD TRANSFUSION MICRO-FILTER W/STRAIGHT SE received FDA 510(k) clearance under submission number K855064, sponsored by Cobe Laboratories, 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 1986-03-12.

Classification & Regulation

This clearance is catalogued under FDA product code CAK and 21 CFR 880.5440, within the General Hospital review panel as a Class II device.