meddevicedb.com FDA Device Reference

SIGNATURE(TM) CUSTOM TUBING PACK

K924529 Class II Traditional
Decision Date
1993-06-23
Sponsor / Applicant
Avecor Cardiovascular, Inc.

Technical Specification

510(k) Submission ID K924529
Product Code DWF
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4210
Decision Date 1993-06-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SIGNATURE(TM) CUSTOM TUBING PACK received FDA 510(k) clearance under submission number K924529, sponsored by Avecor Cardiovascular, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1993-06-23.

Classification & Regulation

This clearance is catalogued under FDA product code DWF and 21 CFR 870.4210, within the Cardiovascular review panel as a Class II device.