meddevicedb.com FDA Device Reference

HIGH STOY SMALL PARTS SCANNER #SP-100B

K800850 Class II Traditional
Decision Date
1980-07-21
Sponsor / Applicant
Highstoy

Technical Specification

510(k) Submission ID K800850
Product Code DXK
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2330
Decision Date 1980-07-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HIGH STOY SMALL PARTS SCANNER #SP-100B received FDA 510(k) clearance under submission number K800850, sponsored by Highstoy. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1980-07-21.

Classification & Regulation

This clearance is catalogued under FDA product code DXK and 21 CFR 870.2330, within the Cardiovascular review panel as a Class II device.