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OPERAID DISPOS. IRRIGATING KNIFE

K845039 Class I Traditional
Decision Date
1985-03-05
Sponsor / Applicant
Jedmed Instrument Co.

Technical Specification

510(k) Submission ID K845039
Product Code KYG
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4360
Decision Date 1985-03-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OPERAID DISPOS. IRRIGATING KNIFE received FDA 510(k) clearance under submission number K845039, sponsored by Jedmed Instrument Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1985-03-05.

Classification & Regulation

This clearance is catalogued under FDA product code KYG and 21 CFR 886.4360, within the Ophthalmic review panel as a Class I device.