meddevicedb.com FDA Device Reference

ZERO GRAVITY WHEELCHAIR COMPONENTS, MODIFICATION

K933051 Class I Traditional
Decision Date
1993-10-12
Sponsor / Applicant
General Components Intl., Inc.

Technical Specification

510(k) Submission ID K933051
Product Code KNN
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3920
Decision Date 1993-10-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ZERO GRAVITY WHEELCHAIR COMPONENTS, MODIFICATION received FDA 510(k) clearance under submission number K933051, sponsored by General Components Intl., Inc.. 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 1993-10-12.

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.