meddevicedb.com FDA Device Reference

LIC TILT BED

K830633 Class I Traditional
Decision Date
1983-03-10
Sponsor / Applicant
Century Manufacturing Co.

Technical Specification

510(k) Submission ID K830633
Product Code INQ
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3760
Decision Date 1983-03-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LIC TILT BED received FDA 510(k) clearance under submission number K830633, sponsored by Century Manufacturing Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 1983-03-10.

Classification & Regulation

This clearance is catalogued under FDA product code INQ and 21 CFR 890.3760, within the Physical Medicine review panel as a Class I device.