meddevicedb.com FDA Device Reference

CALM CURVE, VERSION 01.00

K052715 Class II Special
Decision Date
2005-12-22
Sponsor / Applicant
Lms Medical Systems (Canada), Ltd.

Technical Specification

510(k) Submission ID K052715
Product Code HGM
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.2740
Decision Date 2005-12-22
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CALM CURVE, VERSION 01.00 received FDA 510(k) clearance under submission number K052715, sponsored by Lms Medical Systems (Canada), Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2005-12-22.

Classification & Regulation

This clearance is catalogued under FDA product code HGM and 21 CFR 884.2740, within the Obstetrics/Gynecology review panel as a Class II device.