meddevicedb.com FDA Device Reference

17-900 TO 17-980 VARIOUS TOWEL CLAMPS

K851774 Class I Traditional
Decision Date
1985-06-20
Sponsor / Applicant
Artiberia

Technical Specification

510(k) Submission ID K851774
Product Code GDJ
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1985-06-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

17-900 TO 17-980 VARIOUS TOWEL CLAMPS received FDA 510(k) clearance under submission number K851774, sponsored by Artiberia. 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 1985-06-20.

Classification & Regulation

This clearance is catalogued under FDA product code GDJ and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.