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STC DIAGNOSTIC 8000

K935368 Class II Traditional
Decision Date
1995-05-01
Sponsor / Applicant
Sherman Technology Corp.

Technical Specification

510(k) Submission ID K935368
Product Code IKN
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.1375
Decision Date 1995-05-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STC DIAGNOSTIC 8000 received FDA 510(k) clearance under submission number K935368, sponsored by Sherman Technology 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 1995-05-01.

Classification & Regulation

This clearance is catalogued under FDA product code IKN and 21 CFR 890.1375, within the Physical Medicine review panel as a Class II device.