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MICRO SURGICAL HANDLE

K831996 Class I Traditional
Decision Date
1983-07-12
Sponsor / Applicant
Visitec Co.

Technical Specification

510(k) Submission ID K831996
Product Code KYG
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4360
Decision Date 1983-07-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MICRO SURGICAL HANDLE received FDA 510(k) clearance under submission number K831996, sponsored by Visitec 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 1983-07-12.

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.