meddevicedb.com FDA Device Reference

A-V MINI CLINIC

K800405 Class II Traditional
Decision Date
1980-07-21
Sponsor / Applicant
Instromedix, Inc.

Technical Specification

510(k) Submission ID K800405
Product Code DRT
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2300
Decision Date 1980-07-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

A-V MINI CLINIC received FDA 510(k) clearance under submission number K800405, sponsored by Instromedix, Inc.. 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 DRT and 21 CFR 870.2300, within the Cardiovascular review panel as a Class II device.