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CENTURA PHOTOTHERAPY SPOTLIGHT

K010495 Class II Traditional
Decision Date
2001-03-09
Sponsor / Applicant
Medical Illumination International, Inc.

Technical Specification

510(k) Submission ID K010495
Product Code LBI
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5700
Decision Date 2001-03-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CENTURA PHOTOTHERAPY SPOTLIGHT received FDA 510(k) clearance under submission number K010495, sponsored by Medical Illumination International, Inc.. 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 2001-03-09.

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.