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MDT SHAMPAINE 5100B AND 5100E SURGICAL TABLES

K941150 Class I Traditional
Decision Date
1994-06-10
Sponsor / Applicant
Mdt Technology For Life

Technical Specification

510(k) Submission ID K941150
Product Code FQO
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4960
Decision Date 1994-06-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MDT SHAMPAINE 5100B AND 5100E SURGICAL TABLES received FDA 510(k) clearance under submission number K941150, sponsored by Mdt Technology For Life. 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 1994-06-10.

Classification & Regulation

This clearance is catalogued under FDA product code FQO and 21 CFR 878.4960, within the General, Plastic Surgery review panel as a Class I device.