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CHURCHILL ALBUMIN IV ADMINISTRATION SET

K872124 Class II Traditional
Decision Date
1987-10-13
Sponsor / Applicant
Churchill Corp.

Technical Specification

510(k) Submission ID K872124
Product Code FPA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 1987-10-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CHURCHILL ALBUMIN IV ADMINISTRATION SET received FDA 510(k) clearance under submission number K872124, sponsored by Churchill Corp.. 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 1987-10-13.

Classification & Regulation

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