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POCKET ULTRASONIC PACHYMETER

K993674 Class II Traditional
Decision Date
2000-07-13
Sponsor / Applicant
Quantel Medical

Technical Specification

510(k) Submission ID K993674
Product Code IYO
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1560
Decision Date 2000-07-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POCKET ULTRASONIC PACHYMETER received FDA 510(k) clearance under submission number K993674, sponsored by Quantel Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2000-07-13.

Classification & Regulation

This clearance is catalogued under FDA product code IYO and 21 CFR 892.1560, within the Radiology review panel as a Class II device.