meddevicedb.com FDA Device Reference

ULTRAFLOTATION MEDICAL WHEELCHAIR

K884908 Class I Traditional
Decision Date
1988-12-27
Sponsor / Applicant
Medical Flotation Systems, Inc.

Technical Specification

510(k) Submission ID K884908
Product Code INF
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3940
Decision Date 1988-12-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ULTRAFLOTATION MEDICAL WHEELCHAIR received FDA 510(k) clearance under submission number K884908, sponsored by Medical Flotation Systems, 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 1988-12-27.

Classification & Regulation

This clearance is catalogued under FDA product code INF and 21 CFR 890.3940, within the Physical Medicine review panel as a Class I device.