FDA 510(k)

1.5T AND 3T 8-CHANNEL MEDIUM GENERAL PURPOSE FLEX COIL

K-Number: K111673 · 2011-12-23

Decision Date2011-12-23

Product CodeMOS

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

1.5T AND 3T 8-CHANNEL MEDIUM GENERAL PURPOSE FLEX COIL is the device name listed in this FDA 510(k) record. The listed applicant is Invivo Corporation. It received FDA 510(k) clearance on 2011-12-23 under 510(k) number K111673. 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 1.5T AND 3T 8-CHANNEL MEDIUM GENERAL PURPOSE FLEX COIL?

1.5T AND 3T 8-CHANNEL MEDIUM GENERAL PURPOSE FLEX COIL is a medical device that received FDA 510(k) clearance on 2011-12-23. The listed applicant is Invivo Corporation. The 510(k) number is K111673.

When did 1.5T AND 3T 8-CHANNEL MEDIUM GENERAL PURPOSE FLEX COIL receive FDA 510(k) clearance?

1.5T AND 3T 8-CHANNEL MEDIUM GENERAL PURPOSE FLEX COIL received FDA 510(k) clearance on 2011-12-23, under 510(k) number K111673.

Who is the listed applicant for 1.5T AND 3T 8-CHANNEL MEDIUM GENERAL PURPOSE FLEX COIL?

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 1.5T AND 3T 8-CHANNEL MEDIUM GENERAL PURPOSE FLEX COIL?

The FDA product code for 1.5T AND 3T 8-CHANNEL MEDIUM GENERAL PURPOSE FLEX COIL is MOS.

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Related Devices (Code: MOS)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.