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THERAPY SCOOTER

K780296 Class I Traditional
Decision Date
1978-02-24
Sponsor / Applicant
Convaid Product Development

Technical Specification

510(k) Submission ID K780296
Product Code KNL
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5370
Decision Date 1978-02-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

THERAPY SCOOTER received FDA 510(k) clearance under submission number K780296, sponsored by Convaid Product Development. 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 1978-02-24.

Classification & Regulation

This clearance is catalogued under FDA product code KNL and 21 CFR 890.5370, within the Physical Medicine review panel as a Class I device.