meddevicedb.com FDA Device Reference

RECORDER, RE-100P HOT STYLUS STRIP CHART

K780245 Class I Traditional
Decision Date
1978-03-27
Sponsor / Applicant
Waters Assoc., Inc.

Technical Specification

510(k) Submission ID K780245
Product Code DSF
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2810
Decision Date 1978-03-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RECORDER, RE-100P HOT STYLUS STRIP CHART received FDA 510(k) clearance under submission number K780245, sponsored by Waters Assoc., 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 1978-03-27.

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.