meddevicedb.com FDA Device Reference

POWER EXAMINATION TABLE MODEL # 411

K894134 Class I Traditional
Decision Date
1989-08-28
Sponsor / Applicant
Midmark Corp.

Technical Specification

510(k) Submission ID K894134
Product Code LGX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4960
Decision Date 1989-08-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POWER EXAMINATION TABLE MODEL # 411 received FDA 510(k) clearance under submission number K894134, sponsored by Midmark 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 1989-08-28.

Classification & Regulation

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