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FDA 510(k)

NEOCOIL 3.0T 6-CHANNEL CAROTID ARRAY COIL

K-Number: K070778 · 2007-04-11

ApplicantNeocoil
Decision Date2007-04-11
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

NEOCOIL 3.0T 6-CHANNEL CAROTID ARRAY COIL is the device name listed in this FDA 510(k) record. The listed applicant is Neocoil. It received FDA 510(k) clearance on 2007-04-11 under 510(k) number K070778. 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 NEOCOIL 3.0T 6-CHANNEL CAROTID ARRAY COIL?

NEOCOIL 3.0T 6-CHANNEL CAROTID ARRAY COIL is a medical device that received FDA 510(k) clearance on 2007-04-11. The listed applicant is Neocoil. The 510(k) number is K070778.

When did NEOCOIL 3.0T 6-CHANNEL CAROTID ARRAY COIL receive FDA 510(k) clearance?

NEOCOIL 3.0T 6-CHANNEL CAROTID ARRAY COIL received FDA 510(k) clearance on 2007-04-11, under 510(k) number K070778.

Who is the listed applicant for NEOCOIL 3.0T 6-CHANNEL CAROTID ARRAY COIL?

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

What is the FDA product code for NEOCOIL 3.0T 6-CHANNEL CAROTID ARRAY COIL?

The FDA product code for NEOCOIL 3.0T 6-CHANNEL CAROTID ARRAY COIL is MOS.

Related Clinical Trials

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.

Other records listing Neocoil as applicant

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.

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.

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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