meddevicedb.com FDA Device Reference

VS Tabletop Tonometer

K223739 Class II Traditional
Decision Date
2023-11-08
Sponsor / Applicant
Medimaging Integrated Solution, Inc.

Technical Specification

510(k) Submission ID K223739
Product Code HKX
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1930
Decision Date 2023-11-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VS Tabletop Tonometer received FDA 510(k) clearance under submission number K223739, sponsored by Medimaging Integrated Solution, 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 2023-11-08.

Classification & Regulation

This clearance is catalogued under FDA product code HKX and 21 CFR 886.1930, within the Ophthalmic review panel as a Class II device.