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NEONATAL PHOTOTHERAPY UNIT

K802702 Class II Traditional
Decision Date
1980-12-10
Sponsor / Applicant
Ohio Medical Products

Technical Specification

510(k) Submission ID K802702
Product Code LBI
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5700
Decision Date 1980-12-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NEONATAL PHOTOTHERAPY UNIT received FDA 510(k) clearance under submission number K802702, sponsored by Ohio Medical Products. 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 1980-12-10.

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.