meddevicedb.com FDA Device Reference

TILT TYPE AC POWERED HOSPITAL BED

K780371 Class II Traditional
Decision Date
1978-04-10
Sponsor / Applicant
Medical Specialty Products, Inc.

Technical Specification

510(k) Submission ID K780371
Product Code FNL
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5100
Decision Date 1978-04-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TILT TYPE AC POWERED HOSPITAL BED received FDA 510(k) clearance under submission number K780371, sponsored by Medical Specialty Products, 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 1978-04-10.

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.