meddevicedb.com FDA Device Reference

OPERATING ROOM TABLES HYDRAULIC

K832340 Class I Traditional
Decision Date
1983-08-12
Sponsor / Applicant
Kamiya Tsusan Kaisha, Ltd.

Technical Specification

510(k) Submission ID K832340
Product Code BWN
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4950
Decision Date 1983-08-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OPERATING ROOM TABLES HYDRAULIC received FDA 510(k) clearance under submission number K832340, sponsored by Kamiya Tsusan Kaisha, Ltd.. 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 1983-08-12.

Classification & Regulation

This clearance is catalogued under FDA product code BWN and 21 CFR 878.4950, within the General, Plastic Surgery review panel as a Class I device.