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TINY HALOGEN EXAM LIGHT

K896962 Class I Traditional
Decision Date
1989-12-29
Sponsor / Applicant
Jedmed Instrument Co.

Technical Specification

510(k) Submission ID K896962
Product Code KZF
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6320
Decision Date 1989-12-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TINY HALOGEN EXAM LIGHT received FDA 510(k) clearance under submission number K896962, sponsored by Jedmed Instrument Co.. 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 1989-12-29.

Classification & Regulation

This clearance is catalogued under FDA product code KZF and 21 CFR 880.6320, within the General Hospital review panel as a Class I device.