meddevicedb.com FDA Device Reference

LINDE OXYGEN CONCENTRATOR MODEL LOC-HC

K791043 Class II Traditional
Decision Date
1979-06-13
Sponsor / Applicant
Union Carbide Corp.

Technical Specification

510(k) Submission ID K791043
Product Code CAW
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.5440
Decision Date 1979-06-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LINDE OXYGEN CONCENTRATOR MODEL LOC-HC received FDA 510(k) clearance under submission number K791043, sponsored by Union Carbide Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 1979-06-13.

Classification & Regulation

This clearance is catalogued under FDA product code CAW and 21 CFR 868.5440, within the Anesthesiology review panel as a Class II device.