meddevicedb.com FDA Device Reference

PUSH CUSH

K864108 Class I Traditional
Decision Date
1986-11-14
Sponsor / Applicant
Medical Industries America, Inc.

Technical Specification

510(k) Submission ID K864108
Product Code KIC
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3175
Decision Date 1986-11-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PUSH CUSH received FDA 510(k) clearance under submission number K864108, sponsored by Medical Industries America, 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 1986-11-14.

Classification & Regulation

This clearance is catalogued under FDA product code KIC and 21 CFR 890.3175, within the Physical Medicine review panel as a Class I device.