meddevicedb.com FDA Device Reference

SURGI-CUF STERILE/NON-STERILE DISPOSABLE

K883977 Class II Traditional
Decision Date
1989-02-10
Sponsor / Applicant
Ethox Corp.

Technical Specification

510(k) Submission ID K883977
Product Code DXQ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1120
Decision Date 1989-02-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURGI-CUF STERILE/NON-STERILE DISPOSABLE received FDA 510(k) clearance under submission number K883977, sponsored by Ethox Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1989-02-10.

Classification & Regulation

This clearance is catalogued under FDA product code DXQ and 21 CFR 870.1120, within the Cardiovascular review panel as a Class II device.