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FDA 510(k)

Mural Perinatal Surveillance

K-Number: K220732 · 2022-06-23

ApplicantGe Medical Systems Information Technologies, Inc.
Decision Date2022-06-23
Product CodeHGM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Mural Perinatal Surveillance is the device name listed in this FDA 510(k) record. The listed applicant is Ge Medical Systems Information Technologies, Inc.. It received FDA 510(k) clearance on 2022-06-23 under 510(k) 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. The listed applicant is Ge Medical Systems Information Technologies, Inc.. The 510(k) number is K220732.

When did Mural Perinatal Surveillance receive FDA 510(k) clearance?

Mural Perinatal Surveillance received FDA 510(k) clearance on 2022-06-23, under 510(k) number K220732.

Who is the listed applicant for Mural Perinatal Surveillance?

The FDA 510(k) record lists Ge Medical Systems Information Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Mural Perinatal Surveillance?

The FDA product code for Mural Perinatal Surveillance is HGM.

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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.

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