Mural Perinatal Surveillance
K-Number: K220732 · 2022-06-23
Decision Date2022-06-23
Product CodeHGM
Advisory CommitteeOB
DecisionSubstantially Equivalent
Device Summary
Mural Perinatal Surveillance is a medical device manufactured by Ge Medical Systems Information Technologies, Inc.. It received FDA 510(k) clearance on 2022-06-23 under approval number K220732. The device is classified under product code HGM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Mural Perinatal Surveillance?
Mural Perinatal Surveillance is a medical device that received FDA 510(k) clearance on 2022-06-23. It is manufactured by Ge Medical Systems Information Technologies, Inc.. The 510(k) number is K220732.
When was Mural Perinatal Surveillance approved by the FDA?
Mural Perinatal Surveillance received FDA 510(k) clearance on 2022-06-23, under approval number K220732.
What company makes Mural Perinatal Surveillance?
Mural Perinatal Surveillance is manufactured by Ge Medical Systems Information Technologies, Inc..
What is the FDA product code for Mural Perinatal Surveillance?
The FDA product code for Mural Perinatal Surveillance is HGM.
Other Devices by Ge Medical Systems Information Technologies, Inc.
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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.