meddevicedb.com FDA Device Reference

WEIGHING STATION, MOBILE PATIENT

K760545 Class I Traditional
Decision Date
1976-11-12
Sponsor / Applicant
Gaymar Industries, Inc.

Technical Specification

510(k) Submission ID K760545
Product Code FRW
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2720
Decision Date 1976-11-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WEIGHING STATION, MOBILE PATIENT received FDA 510(k) clearance under submission number K760545, sponsored by Gaymar Industries, 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 1976-11-12.

Classification & Regulation

This clearance is catalogued under FDA product code FRW and 21 CFR 880.2720, within the General Hospital review panel as a Class I device.