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FDA 510(k)

BRUKER R28 WHOLE-BODY MR SCANNER

K-Number: K900026 · 1990-04-30

Decision Date1990-04-30
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BRUKER R28 WHOLE-BODY MR SCANNER is the device name listed in this FDA 510(k) record. The listed applicant is Bruker Medical Imaging, Inc.. It received FDA 510(k) clearance on 1990-04-30 under 510(k) number K900026. 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 BRUKER R28 WHOLE-BODY MR SCANNER?

BRUKER R28 WHOLE-BODY MR SCANNER is a medical device that received FDA 510(k) clearance on 1990-04-30. The listed applicant is Bruker Medical Imaging, Inc.. The 510(k) number is K900026.

When did BRUKER R28 WHOLE-BODY MR SCANNER receive FDA 510(k) clearance?

BRUKER R28 WHOLE-BODY MR SCANNER received FDA 510(k) clearance on 1990-04-30, under 510(k) number K900026.

Who is the listed applicant for BRUKER R28 WHOLE-BODY MR SCANNER?

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

What is the FDA product code for BRUKER R28 WHOLE-BODY MR SCANNER?

The FDA product code for BRUKER R28 WHOLE-BODY MR SCANNER is LNH.

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 Bruker Medical Imaging, 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.

View all 7 devices →

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.

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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