meddevicedb.com FDA Device Reference

TRICYCLES

K862895 Class I Traditional
Decision Date
1986-08-13
Sponsor / Applicant
Mednet, Inc.

Technical Specification

510(k) Submission ID K862895
Product Code IKX
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5050
Decision Date 1986-08-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRICYCLES received FDA 510(k) clearance under submission number K862895, sponsored by Mednet, 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 1986-08-13.

Classification & Regulation

This clearance is catalogued under FDA product code IKX and 21 CFR 890.5050, within the Physical Medicine review panel as a Class I device.