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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 the device name listed in this FDA 510(k) record. The listed applicant is Nova Medical, Inc.. It received FDA 510(k) clearance on 2019-04-12 under 510(k) 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. The listed applicant is Nova Medical, Inc.. The 510(k) number is K182737.

When did 3T 32 Channel Head Coil receive FDA 510(k) clearance?

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

Who is the listed applicant for 3T 32 Channel Head Coil?

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

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

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

Related Devices (Code: MOS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.

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