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FDA 510(k)

3T 32 Channel Head Coil

K-Number: K182737 · 2019-04-12

ApplicantNova Medical, Inc.
Decision Date2019-04-12
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

3T 32 Channel Head Coil is a medical device manufactured by Nova Medical, Inc.. It received FDA 510(k) clearance on 2019-04-12 under approval number K182737. 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 3T 32 Channel Head Coil?

3T 32 Channel Head Coil is a medical device that received FDA 510(k) clearance on 2019-04-12. It is manufactured by Nova Medical, Inc.. The 510(k) number is K182737.

When was 3T 32 Channel Head Coil approved by the FDA?

3T 32 Channel Head Coil received FDA 510(k) clearance on 2019-04-12, under approval number K182737.

What company makes 3T 32 Channel Head Coil?

3T 32 Channel Head Coil is manufactured by Nova Medical, Inc..

What is the FDA product code for 3T 32 Channel Head Coil?

The FDA product code for 3T 32 Channel Head Coil is MOS.

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Official Source

View on FDA Database →

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