COOK Vacuum Pump
K-Number: K160753 · 2017-06-13
Decision Date2017-06-13
Product CodeMQG
Advisory CommitteeOB
DecisionSubstantially Equivalent
Device Summary
COOK Vacuum Pump is a medical device manufactured by William A. Cook Australia Pty. , Ltd.. It received FDA 510(k) clearance on 2017-06-13 under approval number K160753. 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 COOK Vacuum Pump?
COOK Vacuum Pump is a medical device that received FDA 510(k) clearance on 2017-06-13. It is manufactured by William A. Cook Australia Pty. , Ltd.. The 510(k) number is K160753.
When was COOK Vacuum Pump approved by the FDA?
COOK Vacuum Pump received FDA 510(k) clearance on 2017-06-13, under approval number K160753.
What company makes COOK Vacuum Pump?
COOK Vacuum Pump is manufactured by William A. Cook Australia Pty. , Ltd..
What is the FDA product code for COOK Vacuum Pump?
The FDA product code for COOK Vacuum Pump is MQG.
Other Devices by William A. Cook Australia Pty. , Ltd.
K153478Sydney IVF Gamete Buffer
K152717Sydney IVF Blastocyst Cryopreservation Kit, Sydney IVF Blastocyst Thawing Kit
K160814Sydney IVF Sperm Cryopreservation Buffer
K151367Sydney IVF Hyaluronidase
K153290Sydney IVF Follicle Flush Buffer, Sydney IVF Fertilization Medium, Sydney IVF Cleavage Medium, Sydney IVF Blastocyst Medium
K171611Double Lumen Ovum Aspiration Needles
Related Devices (Code: MQG)
K160504RI Witness Embryology Heated PlateResearch Instruments Limited
K151357MIRI TLAt Medical Uab
K171736Geri Embryo Incubator and Geri DishGenea Biomedx 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.