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HEEL OR ELBOW PROTECTOR

K812344 Class I Traditional
Decision Date
1981-09-11
Sponsor / Applicant
Fred Sammons, Inc.

Technical Specification

510(k) Submission ID K812344
Product Code FMP
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6450
Decision Date 1981-09-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEEL OR ELBOW PROTECTOR received FDA 510(k) clearance under submission number K812344, sponsored by Fred Sammons, 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 1981-09-11.

Classification & Regulation

This clearance is catalogued under FDA product code FMP and 21 CFR 880.6450, within the General Hospital review panel as a Class I device.