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ELBOW PROTECTOR

K780171 Class I Traditional
Decision Date
1978-02-06
Sponsor / Applicant
Stat Medical Corp.

Technical Specification

510(k) Submission ID K780171
Product Code FMP
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6450
Decision Date 1978-02-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELBOW PROTECTOR received FDA 510(k) clearance under submission number K780171, sponsored by Stat Medical Corp.. 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 1978-02-06.

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.