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CHAIN KIT

K823875 Class I Traditional
Decision Date
1983-01-14
Sponsor / Applicant
Berkeley Electric Wheelchair Co.

Technical Specification

510(k) Submission ID K823875
Product Code KNN
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3920
Decision Date 1983-01-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CHAIN KIT received FDA 510(k) clearance under submission number K823875, sponsored by Berkeley Electric Wheelchair Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 1983-01-14.

Classification & Regulation

This clearance is catalogued under FDA product code KNN and 21 CFR 890.3920, within the Physical Medicine review panel as a Class I device.