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OHMEDA MEDICAL SPOT PT LITE PHOTOTHERAPY SYSTEM

K011549 Class II Traditional
Decision Date
2001-07-19
Sponsor / Applicant
Ohmeda Medical

Technical Specification

510(k) Submission ID K011549
Product Code LBI
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5700
Decision Date 2001-07-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OHMEDA MEDICAL SPOT PT LITE PHOTOTHERAPY SYSTEM received FDA 510(k) clearance under submission number K011549, sponsored by Ohmeda Medical. 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 2001-07-19.

Classification & Regulation

This clearance is catalogued under FDA product code LBI and 21 CFR 880.5700, within the General Hospital review panel as a Class II device.