meddevicedb.com FDA Device Reference

TRAY DOUGH

K911225 Class I Traditional
Decision Date
1991-04-17
Sponsor / Applicant
The Hygenic Corp.

Technical Specification

510(k) Submission ID K911225
Product Code KGS
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4930
Decision Date 1991-04-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRAY DOUGH received FDA 510(k) clearance under submission number K911225, sponsored by The Hygenic Corp.. 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 1991-04-17.

Classification & Regulation

This clearance is catalogued under FDA product code KGS and 21 CFR 878.4930, within the General, Plastic Surgery review panel as a Class I device.