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FDA 510(k)

MULTIPURPOSE COIL & 3MM SLICE THICKNESS ON THE MRI

K-Number: K901620 · 1990-05-07

ApplicantInstrumentarium Imaging, Inc.
Decision Date1990-05-07
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MULTIPURPOSE COIL & 3MM SLICE THICKNESS ON THE MRI is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentarium Imaging, Inc.. It received FDA 510(k) clearance on 1990-05-07 under 510(k) number K901620. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTIPURPOSE COIL & 3MM SLICE THICKNESS ON THE MRI?

MULTIPURPOSE COIL & 3MM SLICE THICKNESS ON THE MRI is a medical device that received FDA 510(k) clearance on 1990-05-07. The listed applicant is Instrumentarium Imaging, Inc.. The 510(k) number is K901620.

When did MULTIPURPOSE COIL & 3MM SLICE THICKNESS ON THE MRI receive FDA 510(k) clearance?

MULTIPURPOSE COIL & 3MM SLICE THICKNESS ON THE MRI received FDA 510(k) clearance on 1990-05-07, under 510(k) number K901620.

Who is the listed applicant for MULTIPURPOSE COIL & 3MM SLICE THICKNESS ON THE MRI?

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

What is the FDA product code for MULTIPURPOSE COIL & 3MM SLICE THICKNESS ON THE MRI?

The FDA product code for MULTIPURPOSE COIL & 3MM SLICE THICKNESS ON THE MRI is LNH.

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Related Devices (Code: LNH)

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

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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