meddevicedb.com FDA Device Reference

PNEUMATIC/ELECTRIC/HYDRAULIC BED

K831821 Class II Traditional
Decision Date
1983-08-08
Sponsor / Applicant
G.W. Healthcare, Inc.

Technical Specification

510(k) Submission ID K831821
Product Code FNL
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5100
Decision Date 1983-08-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PNEUMATIC/ELECTRIC/HYDRAULIC BED received FDA 510(k) clearance under submission number K831821, sponsored by G.W. Healthcare, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1983-08-08.

Classification & Regulation

This clearance is catalogued under FDA product code FNL and 21 CFR 880.5100, within the General Hospital review panel as a Class II device.