meddevicedb.com FDA Device Reference

'cottony' II TAPE, PLEDGETS

K153089 Class II Traditional
Decision Date
2016-08-12
Sponsor / Applicant
Teleflexmedical, Inc.

Technical Specification

510(k) Submission ID K153089
Product Code GAT
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5000
Decision Date 2016-08-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

'cottony' II TAPE, PLEDGETS received FDA 510(k) clearance under submission number K153089, sponsored by Teleflexmedical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2016-08-12.

Classification & Regulation

This clearance is catalogued under FDA product code GAT and 21 CFR 878.5000, within the General, Plastic Surgery review panel as a Class II device.