DeviceClearance

Product code LHZ— Obstetrics/Gynecology

SALTIME VISCOMETER

Classification name
Viscometer, Mucus, Cervical
Device class
Class 1
Regulation
21 CFR 884.1040
Advisory panel
Obstetrics/Gynecology
Total cleared
1
First cleared
Most recent

Market context for product code LHZ

FDA has cleared 1 device under product code LHZ, all in 1996, filed by 1 applicant company. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

Top applicants under product code LHZ

Recent clearances under product code LHZ

Data sourced from openFDA. This site is unofficial and independent of the FDA.