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REVISED LABELING FOR CHROMIC AND PLAIN GUT SUTURES

K926586 Class II Traditional
Decision Date
1993-12-22
Sponsor / Applicant
Look, Inc.

Technical Specification

510(k) Submission ID K926586
Product Code GAL
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4830
Decision Date 1993-12-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

REVISED LABELING FOR CHROMIC AND PLAIN GUT SUTURES received FDA 510(k) clearance under submission number K926586, sponsored by Look, 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 1993-12-22.

Classification & Regulation

This clearance is catalogued under FDA product code GAL and 21 CFR 878.4830, within the General, Plastic Surgery review panel as a Class II device.