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CHURCHILL MEDICAL DUAL CHAMBER EMPTY CONTAINER

K041038 Class II Abbreviated
Decision Date
2004-12-21
Sponsor / Applicant
Churchill Medical Systems, Inc.

Technical Specification

510(k) Submission ID K041038
Product Code KPE
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5025
Decision Date 2004-12-21
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CHURCHILL MEDICAL DUAL CHAMBER EMPTY CONTAINER received FDA 510(k) clearance under submission number K041038, sponsored by Churchill Medical Systems, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2004-12-21.

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.