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FDA 510(k)

SENSE MSK S 8CH 1.5T

K-Number: K120122 · 2012-02-10

ApplicantInvivo Corporation
Decision Date2012-02-10
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SENSE MSK S 8CH 1.5T is the device name listed in this FDA 510(k) record. The listed applicant is Invivo Corporation. It received FDA 510(k) clearance on 2012-02-10 under 510(k) number K120122. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SENSE MSK S 8CH 1.5T?

SENSE MSK S 8CH 1.5T is a medical device that received FDA 510(k) clearance on 2012-02-10. The listed applicant is Invivo Corporation. The 510(k) number is K120122.

When did SENSE MSK S 8CH 1.5T receive FDA 510(k) clearance?

SENSE MSK S 8CH 1.5T received FDA 510(k) clearance on 2012-02-10, under 510(k) number K120122.

Who is the listed applicant for SENSE MSK S 8CH 1.5T?

The FDA 510(k) record lists Invivo Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SENSE MSK S 8CH 1.5T?

The FDA product code for SENSE MSK S 8CH 1.5T is MOS.

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Related Devices (Code: MOS)

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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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