meddevicedb.com FDA Device Reference

WORK SIMULATOR

K800007 Class I Traditional
Decision Date
1980-01-21
Sponsor / Applicant
Baltimore Therapeutic Equipment Co.

Technical Specification

510(k) Submission ID K800007
Product Code BXB
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5380
Decision Date 1980-01-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WORK SIMULATOR received FDA 510(k) clearance under submission number K800007, sponsored by Baltimore Therapeutic Equipment Co.. 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 1980-01-21.

Classification & Regulation

This clearance is catalogued under FDA product code BXB and 21 CFR 890.5380, within the Physical Medicine review panel as a Class I device.