meddevicedb.com FDA Device Reference

THE MEDIC TM

K920912 Class II Traditional
Decision Date
1993-07-30
Sponsor / Applicant
Medical and Environment Designs, Inc.

Technical Specification

510(k) Submission ID K920912
Product Code GCX
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6740
Decision Date 1993-07-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

THE MEDIC TM received FDA 510(k) clearance under submission number K920912, sponsored by Medical and Environment Designs, Inc.. 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 1993-07-30.

Classification & Regulation

This clearance is catalogued under FDA product code GCX and 21 CFR 880.6740, within the General Hospital review panel as a Class II device.