meddevicedb.com FDA Device Reference

COVIDIEN EXTENDED TIP APPLICATOR

K091315 Class II Special
Decision Date
2009-06-05
Sponsor / Applicant
Confluent Surgical,Inc

Technical Specification

510(k) Submission ID K091315
Product Code FMF
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5860
Decision Date 2009-06-05
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COVIDIEN EXTENDED TIP APPLICATOR received FDA 510(k) clearance under submission number K091315, sponsored by Confluent Surgical,Inc. The device was reviewed via the Special premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2009-06-05.

Classification & Regulation

This clearance is catalogued under FDA product code FMF and 21 CFR 880.5860, within the General Hospital review panel as a Class II device.