meddevicedb.com FDA Device Reference

MED-RX EXTENSION SET WITH T-CONNECTOR

K112799 Class II Traditional
Decision Date
2011-12-23
Sponsor / Applicant
Benlan, Inc.

Technical Specification

510(k) Submission ID K112799
Product Code FPA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 2011-12-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MED-RX EXTENSION SET WITH T-CONNECTOR received FDA 510(k) clearance under submission number K112799, sponsored by Benlan, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2011-12-23.

Classification & Regulation

This clearance is catalogued under FDA product code FPA and 21 CFR 880.5440, within the General Hospital review panel as a Class II device.