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FDA 510(k)

USA INSTRUMENTS 3.0T BRAIN/SPINE ARRAY

K-Number: K052916 · 2005-11-09

ApplicantUsa Instruments, Inc.
Decision Date2005-11-09
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

USA INSTRUMENTS 3.0T BRAIN/SPINE ARRAY is the device name listed in this FDA 510(k) record. The listed applicant is Usa Instruments, Inc.. It received FDA 510(k) clearance on 2005-11-09 under 510(k) number K052916. 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 USA INSTRUMENTS 3.0T BRAIN/SPINE ARRAY?

USA INSTRUMENTS 3.0T BRAIN/SPINE ARRAY is a medical device that received FDA 510(k) clearance on 2005-11-09. The listed applicant is Usa Instruments, Inc.. The 510(k) number is K052916.

When did USA INSTRUMENTS 3.0T BRAIN/SPINE ARRAY receive FDA 510(k) clearance?

USA INSTRUMENTS 3.0T BRAIN/SPINE ARRAY received FDA 510(k) clearance on 2005-11-09, under 510(k) number K052916.

Who is the listed applicant for USA INSTRUMENTS 3.0T BRAIN/SPINE ARRAY?

The FDA 510(k) record lists Usa Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for USA INSTRUMENTS 3.0T BRAIN/SPINE ARRAY?

The FDA product code for USA INSTRUMENTS 3.0T BRAIN/SPINE ARRAY is MOS.

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Other records listing Usa Instruments, Inc. as applicant

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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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