meddevicedb.com FDA Device Reference

MICROMED PD-8K INSULATION DEFECT DETECTOR

K101606 Class II Traditional
Decision Date
2010-10-01
Sponsor / Applicant
Mcgan Technology, LLC

Technical Specification

510(k) Submission ID K101606
Product Code HFG
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.4160
Decision Date 2010-10-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MICROMED PD-8K INSULATION DEFECT DETECTOR received FDA 510(k) clearance under submission number K101606, sponsored by Mcgan Technology, LLC. 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 2010-10-01.

Classification & Regulation

This clearance is catalogued under FDA product code HFG and 21 CFR 884.4160, within the Obstetrics/Gynecology review panel as a Class II device.