meddevicedb.com FDA Device Reference

N/A

K970592 Class II Traditional
Decision Date
1997-06-13
Sponsor / Applicant
North American Technical Services Corp.

Technical Specification

510(k) Submission ID K970592
Product Code ILY
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5500
Decision Date 1997-06-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

N/A received FDA 510(k) clearance under submission number K970592, sponsored by North American Technical Services Corp.. 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 1997-06-13.

Classification & Regulation

This clearance is catalogued under FDA product code ILY and 21 CFR 890.5500, within the Physical Medicine review panel as a Class II device.