meddevicedb.com FDA Device Reference

SPORTSIGHT GP

K993586 Class II Traditional
Decision Date
2000-05-22
Sponsor / Applicant
Paragon Vision Sciences

Technical Specification

510(k) Submission ID K993586
Product Code HQD
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5916
Decision Date 2000-05-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPORTSIGHT GP received FDA 510(k) clearance under submission number K993586, sponsored by Paragon Vision Sciences. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2000-05-22.

Classification & Regulation

This clearance is catalogued under FDA product code HQD and 21 CFR 886.5916, within the Ophthalmic review panel as a Class II device.