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MICROLITE WHEELCHAIR

K933919 Class I Traditional
Decision Date
1993-09-30
Sponsor / Applicant
Morgan Technology, Inc.

Technical Specification

510(k) Submission ID K933919
Product Code IOR
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3850
Decision Date 1993-09-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MICROLITE WHEELCHAIR received FDA 510(k) clearance under submission number K933919, sponsored by Morgan Technology, 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 1993-09-30.

Classification & Regulation

This clearance is catalogued under FDA product code IOR and 21 CFR 890.3850, within the Physical Medicine review panel as a Class I device.