meddevicedb.com FDA Device Reference

TRANSTHORACIC/TRANSABDOMINAL-TRAY

K833720 Class I Traditional
Decision Date
1984-05-30
Sponsor / Applicant
Applied Medical Devices, Inc.

Technical Specification

510(k) Submission ID K833720
Product Code GDM
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1984-05-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRANSTHORACIC/TRANSABDOMINAL-TRAY received FDA 510(k) clearance under submission number K833720, sponsored by Applied Medical Devices, 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 1984-05-30.

Classification & Regulation

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