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LIFECARE EMPTY CONTAINER

K771228 Class II Traditional
Decision Date
1977-08-02
Sponsor / Applicant
Abbott Laboratories

Technical Specification

510(k) Submission ID K771228
Product Code KPE
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5025
Decision Date 1977-08-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LIFECARE EMPTY CONTAINER received FDA 510(k) clearance under submission number K771228, sponsored by Abbott Laboratories. 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 1977-08-02.

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.