meddevicedb.com FDA Device Reference

NITRILON CORRECT-TOUCH

K984512 Class I Traditional
Decision Date
1999-07-12
Sponsor / Applicant
Ct Intl.

Technical Specification

510(k) Submission ID K984512
Product Code KGO
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4460
Decision Date 1999-07-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NITRILON CORRECT-TOUCH received FDA 510(k) clearance under submission number K984512, sponsored by Ct Intl.. 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 1999-07-12.

Classification & Regulation

This clearance is catalogued under FDA product code KGO and 21 CFR 878.4460, within the General, Plastic Surgery review panel as a Class I device.