meddevicedb.com FDA Device Reference

MT96000 PAPER CHART RECORDER

K894736 Class I Traditional
Decision Date
1989-12-13
Sponsor / Applicant
Astro-Med, Inc.

Technical Specification

510(k) Submission ID K894736
Product Code DSF
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2810
Decision Date 1989-12-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MT96000 PAPER CHART RECORDER received FDA 510(k) clearance under submission number K894736, sponsored by Astro-Med, 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 1989-12-13.

Classification & Regulation

This clearance is catalogued under FDA product code DSF and 21 CFR 870.2810, within the Cardiovascular review panel as a Class I device.