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MDT/SHAMPAINE MODEL 4900E SURGICAL TABLE

K915393 Class I Traditional
Decision Date
1991-12-17
Sponsor / Applicant
Mdt Corp., Inc.

Technical Specification

510(k) Submission ID K915393
Product Code GDC
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4960
Decision Date 1991-12-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MDT/SHAMPAINE MODEL 4900E SURGICAL TABLE received FDA 510(k) clearance under submission number K915393, sponsored by Mdt Corp., 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 1991-12-17.

Classification & Regulation

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