meddevicedb.com FDA Device Reference

ONSET ACCESS CATHETER SYSTEM

K112629 Class II Traditional
Decision Date
2011-10-11
Sponsor / Applicant
Onset Medical Corporation

Technical Specification

510(k) Submission ID K112629
Product Code DQY
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1250
Decision Date 2011-10-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ONSET ACCESS CATHETER SYSTEM received FDA 510(k) clearance under submission number K112629, sponsored by Onset Medical Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2011-10-11.

Classification & Regulation

This clearance is catalogued under FDA product code DQY and 21 CFR 870.1250, within the Cardiovascular review panel as a Class II device.