meddevicedb.com FDA Device Reference

TUBING EXTENSION SET

K993361 Class II Traditional
Decision Date
2000-01-04
Sponsor / Applicant
Hurricane Medical

Technical Specification

510(k) Submission ID K993361
Product Code MSR
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4150
Decision Date 2000-01-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TUBING EXTENSION SET received FDA 510(k) clearance under submission number K993361, sponsored by Hurricane Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2000-01-04.

Classification & Regulation

This clearance is catalogued under FDA product code MSR and 21 CFR 886.4150, within the Ophthalmic review panel as a Class II device.