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THE BODY BUGGY

K915361 Class I Traditional
Decision Date
1991-12-20
Sponsor / Applicant
Innova Corp.

Technical Specification

510(k) Submission ID K915361
Product Code LYG
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5660
Decision Date 1991-12-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

THE BODY BUGGY received FDA 510(k) clearance under submission number K915361, sponsored by Innova Corp.. 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 1991-12-20.

Classification & Regulation

This clearance is catalogued under FDA product code LYG and 21 CFR 890.5660, within the Physical Medicine review panel as a Class I device.