meddevicedb.com FDA Device Reference

HSV STRAW

K092398 Class II Traditional
Decision Date
2010-10-06
Sponsor / Applicant
Cryo Bio System

Technical Specification

510(k) Submission ID K092398
Product Code MQK
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.6160
Decision Date 2010-10-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HSV STRAW received FDA 510(k) clearance under submission number K092398, sponsored by Cryo Bio System. 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 2010-10-06.

Classification & Regulation

This clearance is catalogued under FDA product code MQK and 21 CFR 884.6160, within the Obstetrics/Gynecology review panel as a Class II device.