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JEDMED CCD CAMERA SYSTEM

K862664 Class I Traditional
Decision Date
1986-07-30
Sponsor / Applicant
Jedmed Instrument Co.

Technical Specification

510(k) Submission ID K862664
Product Code FWD
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4160
Decision Date 1986-07-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

JEDMED CCD CAMERA SYSTEM received FDA 510(k) clearance under submission number K862664, sponsored by Jedmed Instrument Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1986-07-30.

Classification & Regulation

This clearance is catalogued under FDA product code FWD and 21 CFR 878.4160, within the General, Plastic Surgery review panel as a Class I device.