meddevicedb.com FDA Device Reference

A-SCAN ROLL-AROUND STAND

K900161 Class I Traditional
Decision Date
1990-02-16
Sponsor / Applicant
Jedmed Instrument Co.

Technical Specification

510(k) Submission ID K900161
Product Code HMG
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1860
Decision Date 1990-02-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

A-SCAN ROLL-AROUND STAND received FDA 510(k) clearance under submission number K900161, 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 1990-02-16.

Classification & Regulation

This clearance is catalogued under FDA product code HMG and 21 CFR 886.1860, within the Ophthalmic review panel as a Class I device.