meddevicedb.com FDA Device Reference

IRAS PERIMETER

K864012 Class II Traditional
Decision Date
1986-12-12
Sponsor / Applicant
Randwal Instrument Co., Inc.

Technical Specification

510(k) Submission ID K864012
Product Code HPJ
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1360
Decision Date 1986-12-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IRAS PERIMETER received FDA 510(k) clearance under submission number K864012, sponsored by Randwal Instrument Co., Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1986-12-12.

Classification & Regulation

This clearance is catalogued under FDA product code HPJ and 21 CFR 886.1360, within the Ophthalmic review panel as a Class II device.