meddevicedb.com FDA Device Reference

FPL

K915897 Class I Traditional
Decision Date
1992-04-07
Sponsor / Applicant
Wrm Computers

Technical Specification

510(k) Submission ID K915897
Product Code IKE
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.1615
Decision Date 1992-04-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FPL received FDA 510(k) clearance under submission number K915897, sponsored by Wrm Computers. 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 1992-04-07.

Classification & Regulation

This clearance is catalogued under FDA product code IKE and 21 CFR 890.1615, within the Physical Medicine review panel as a Class I device.