FDA 510(k)

RI Witness Embryology Heated Plate

K-Number: K160504 · 2016-07-18

Decision Date2016-07-18

Product CodeMQG

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

RI Witness Embryology Heated Plate is a medical device manufactured by Research Instruments Limited. It received FDA 510(k) clearance on 2016-07-18 under approval number K160504. The device is classified under product code MQG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RI Witness Embryology Heated Plate?

RI Witness Embryology Heated Plate is a medical device that received FDA 510(k) clearance on 2016-07-18. It is manufactured by Research Instruments Limited. The 510(k) number is K160504.

When was RI Witness Embryology Heated Plate approved by the FDA?

RI Witness Embryology Heated Plate received FDA 510(k) clearance on 2016-07-18, under approval number K160504.

What company makes RI Witness Embryology Heated Plate?

RI Witness Embryology Heated Plate is manufactured by Research Instruments Limited.

What is the FDA product code for RI Witness Embryology Heated Plate?

The FDA product code for RI Witness Embryology Heated Plate is MQG.

Other Devices by Research Instruments Limited

K161275EZ-Tip Singles, EZ-Tip Vial of 20, EZ-Grip

Related Devices (Code: MQG)

K151357MIRI TLAt Medical Uab K171736Geri Embryo Incubator and Geri DishGenea Biomedx Pty, Ltd. K160753COOK Vacuum PumpWilliam A. Cook Australia Pty. , Ltd. K180188Geri Embryo Incubator with Geri Connect and Geri Assess Software, and Geri DishGenea Biomedx Pty, Ltd. K173264EmbryoScope+Vitrolife A/S K180304Geri Embryo Incubator and Geri DishGenea Biomedx Pty, Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.