Product code MQH— Obstetrics/Gynecology

ASSISTED HATCHING MICROPIPETTES, DENUDING PIPETTES, HOLDING MICROPIPETTES, ICSI MICROPIPETTES, PARTIAL ZONE DISSECTION M

Classification name
Microtools, Assisted Reproduction (Pipettes)
Device class
Class 2
Regulation
21 CFR 884.6130
Advisory panel
Obstetrics/Gynecology
Total cleared
26
First cleared
Most recent

Market context for product code MQH

FDA has cleared 26 devices under product code MQH between 1999 and 2025, filed by 19 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Clearances per year

Top applicants under product code MQH

Recent clearances under product code MQH

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