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FDA 510(k)

MC 3003G-32R HEAD COIL

K-Number: K072931 · 2007-10-30

ApplicantMr Instruments, Inc.
Decision Date2007-10-30
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MC 3003G-32R HEAD COIL is the device name listed in this FDA 510(k) record. The listed applicant is Mr Instruments, Inc.. It received FDA 510(k) clearance on 2007-10-30 under 510(k) number K072931. 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 MC 3003G-32R HEAD COIL?

MC 3003G-32R HEAD COIL is a medical device that received FDA 510(k) clearance on 2007-10-30. The listed applicant is Mr Instruments, Inc.. The 510(k) number is K072931.

When did MC 3003G-32R HEAD COIL receive FDA 510(k) clearance?

MC 3003G-32R HEAD COIL received FDA 510(k) clearance on 2007-10-30, under 510(k) number K072931.

Who is the listed applicant for MC 3003G-32R HEAD COIL?

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

What is the FDA product code for MC 3003G-32R HEAD COIL?

The FDA product code for MC 3003G-32R HEAD COIL is MOS.

Other records listing Mr Instruments, Inc. 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.

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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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