meddevicedb.com FDA Device Reference

CUSTOM DRESSING TRAY WET TO DRY

K803117 Class I Traditional
Decision Date
1980-12-23
Sponsor / Applicant
American Medical Disposable, Inc.

Technical Specification

510(k) Submission ID K803117
Product Code KDD
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1980-12-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CUSTOM DRESSING TRAY WET TO DRY received FDA 510(k) clearance under submission number K803117, sponsored by American Medical Disposable, 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 1980-12-23.

Classification & Regulation

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