meddevicedb.com FDA Device Reference

DACA-100

K882933 Class II Traditional
Decision Date
1989-02-08
Sponsor / Applicant
Visual Cybernetics

Technical Specification

510(k) Submission ID K882933
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 1989-02-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DACA-100 received FDA 510(k) clearance under submission number K882933, sponsored by Visual Cybernetics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1989-02-08.

Classification & Regulation

This clearance is catalogued under FDA product code LLZ and 21 CFR 892.2050, within the Radiology review panel as a Class II device.