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OXYGEN-RICH

K760705 Class II Traditional
Decision Date
1976-10-05
Sponsor / Applicant
The John Bunn Co.

Technical Specification

510(k) Submission ID K760705
Product Code CAW
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.5440
Decision Date 1976-10-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OXYGEN-RICH received FDA 510(k) clearance under submission number K760705, sponsored by The John Bunn Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 1976-10-05.

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.