meddevicedb.com FDA Device Reference

GUT SUTURES

K896554 Class II Traditional
Decision Date
1990-05-31
Sponsor / Applicant
Look, Inc.

Technical Specification

510(k) Submission ID K896554
Product Code GAL
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4830
Decision Date 1990-05-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GUT SUTURES received FDA 510(k) clearance under submission number K896554, 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 1990-05-31.

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.