meddevicedb.com FDA Device Reference

APPOSE SKIN STAPLER & REMOVER

K823552 Class II Traditional
Decision Date
1983-06-15
Sponsor / Applicant
American Cyanamid Co.

Technical Specification

510(k) Submission ID K823552
Product Code GDW
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4750
Decision Date 1983-06-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

APPOSE SKIN STAPLER & REMOVER received FDA 510(k) clearance under submission number K823552, sponsored by American Cyanamid Co.. 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 1983-06-15.

Classification & Regulation

This clearance is catalogued under FDA product code GDW and 21 CFR 878.4750, within the General, Plastic Surgery review panel as a Class II device.