meddevicedb.com FDA Device Reference

DECUBITUS CARE PAD

K893969 Class I Traditional
Decision Date
1989-07-14
Sponsor / Applicant
Gulftrade Exim, Inc.

Technical Specification

510(k) Submission ID K893969
Product Code FWZ
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4950
Decision Date 1989-07-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DECUBITUS CARE PAD received FDA 510(k) clearance under submission number K893969, sponsored by Gulftrade Exim, 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 1989-07-14.

Classification & Regulation

This clearance is catalogued under FDA product code FWZ and 21 CFR 878.4950, within the General, Plastic Surgery review panel as a Class I device.