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CDD-PCA(TM) MODEL 5800R AMBULATORY INFUSION PUMP

K911791 Class II Traditional
Decision Date
1991-06-11
Sponsor / Applicant
Pharmacia Deltec, Inc.

Technical Specification

510(k) Submission ID K911791
Product Code MEA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 1991-06-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CDD-PCA(TM) MODEL 5800R AMBULATORY INFUSION PUMP received FDA 510(k) clearance under submission number K911791, sponsored by Pharmacia Deltec, 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 1991-06-11.

Classification & Regulation

This clearance is catalogued under FDA product code MEA and 21 CFR 880.5725, within the General Hospital review panel as a Class II device.