meddevicedb.com FDA Device Reference

ML-800 CO2

K800227 Class II Traditional
Decision Date
1980-03-03
Sponsor / Applicant
Merrimack Laboratories

Technical Specification

510(k) Submission ID K800227
Product Code HHR
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.4550
Decision Date 1980-03-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ML-800 CO2 received FDA 510(k) clearance under submission number K800227, sponsored by Merrimack Laboratories. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 1980-03-03.

Classification & Regulation

This clearance is catalogued under FDA product code HHR and 21 CFR 884.4550, within the Obstetrics/Gynecology review panel as a Class II device.