meddevicedb.com FDA Device Reference

MEDICAL PROCEDURE TRAY

K902410 Traditional
Decision Date
1990-11-20
Sponsor / Applicant
Sorex Medical

Technical Specification

510(k) Submission ID K902410
Product Code LDQ
Medical Specialty / Panel General Hospital
Decision Date 1990-11-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDICAL PROCEDURE TRAY received FDA 510(k) clearance under submission number K902410, sponsored by Sorex Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1990-11-20.

Classification & Regulation

This clearance is catalogued under FDA product code LDQ , within the General Hospital review panel as a device.