meddevicedb.com FDA Device Reference

COMPU-SCAN

K791632 Class II Traditional
Decision Date
1979-11-13
Sponsor / Applicant
Hittman Medical Systems

Technical Specification

510(k) Submission ID K791632
Product Code DSI
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1025
Decision Date 1979-11-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COMPU-SCAN received FDA 510(k) clearance under submission number K791632, sponsored by Hittman Medical Systems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1979-11-13.

Classification & Regulation

This clearance is catalogued under FDA product code DSI and 21 CFR 870.1025, within the Cardiovascular review panel as a Class II device.