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FDA 510(k)

MAGNETIC RESONANCE SYSTEM MODEL BMT-1100

K-Number: K895328 · 1990-03-09

ApplicantBruker Medical Imaging, Inc.
Decision Date1990-03-09
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAGNETIC RESONANCE SYSTEM MODEL BMT-1100 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 1990-03-09 under 510(k) number K895328. 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 MAGNETIC RESONANCE SYSTEM MODEL BMT-1100?

MAGNETIC RESONANCE SYSTEM MODEL BMT-1100 is a medical device that received FDA 510(k) clearance on 1990-03-09. The listed applicant is Bruker Medical Imaging, Inc.. The 510(k) number is K895328.

When did MAGNETIC RESONANCE SYSTEM MODEL BMT-1100 receive FDA 510(k) clearance?

MAGNETIC RESONANCE SYSTEM MODEL BMT-1100 received FDA 510(k) clearance on 1990-03-09, under 510(k) number K895328.

Who is the listed applicant for MAGNETIC RESONANCE SYSTEM MODEL BMT-1100?

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 MAGNETIC RESONANCE SYSTEM MODEL BMT-1100?

The FDA product code for MAGNETIC RESONANCE SYSTEM MODEL BMT-1100 is LNH.

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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.

K915657MODIFIED MAGNETIC RESONANCE IMAGING SYTEM MOD. R28K913463MAG RES IMAG SYST/BRUKER MODEL R28 WHOLE BODY SCANK903661BRUKER R-28,HEAD AND CHEST ANGIOGRAPHY IMAGING ADDK900026BRUKER R28 WHOLE-BODY MR SCANNERK8947141989 SOFTWARE REVISION TO THE BMT-1100K891760MAGNETIC RESONANCE SYSTEM, MODEL BMT 1100,MODIFIED

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Related Devices (Code: LNH)

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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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