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ACCLAIM INFUSION PUMP

K991501 Class II Special
Decision Date
1999-05-13
Sponsor / Applicant
Abbott Laboratories

Technical Specification

510(k) Submission ID K991501
Product Code FRN
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 1999-05-13
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACCLAIM INFUSION PUMP received FDA 510(k) clearance under submission number K991501, sponsored by Abbott Laboratories. The device was reviewed via the Special premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1999-05-13.

Classification & Regulation

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